ML25198A151

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Inspection Manual Chapter 1248 Appendix a Draft for Comment
ML25198A151
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Issue date: 12/16/2025
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NRC INSPECTION MANUAL NMSS INSPECTION MANUAL CHAPTER 1248 APPENDIX A MATERIALS HEALTH PHYSICS LICENSE REVIEWER TRAINING AND QUALIFICATION JOURNAL Effective Date: TBD

Issue Date: XX/XX/25 i

1248 App A TABLE OF CONTENTS INTRODUCTION.......................................................................................................................... 1 PROGRAM ORGANIZATION....................................................................................................... 2 QUALIFICATION JOURNAL ORGANIZATION............................................................................ 2 REQUIRED TRAINING COURSES.............................................................................................. 2 SPECIALIZED TRAINING COURSES.......................................................................................... 3 REFRESHER TRAINING.............................................................................................................. 4 MATERIALS HEALTH PHYSICS LICENSE REVIEWER COMPETENCIES............................... 5 MATERIALS HEALTH PHYSICS LICENSE REVIEWER INDIVIDUAL STUDY ACTIVITY.......... 7 (ISA-1) Web-Based Licensing................................................................................................... 8 (ISA-2) The Role of Agreement States in Radioactive Materials Regulation Under Section 274

................................................................................................................................................ 10 (ISA-3) Reciprocity.................................................................................................................. 13 (ISA-4) Overview of 10 CFR Parts 30 through 39................................................................... 15 (ISA-5) Overview of NUREG-1556.......................................................................................... 18 (ISA-6) Radioactive Materials and Purposes for Which Licensed Material Will Be Used........ 20 (ISA-7) Radiation Safety Officer Training and Experience...................................................... 22 (ISA-8) Training and Experience for Authorized Users, Authorized Nuclear Pharmacist and Authorized Medical Physicist................................................................................................... 24 (ISA-9) Facilities and Equipment............................................................................................. 26 (ISA-10) Radiation Safety Program - Program Audit and Materials Receipt and Accountability

................................................................................................................................................ 28 (ISA-11) Radiation Safety Program - Leak Testing, Radiation Monitoring Equipment and Surveys................................................................................................................................... 30 (ISA-12) Radiation Safety Program - Occupational and Public Dose..................................... 32 (ISA-13) Radiation Safety Program - Operating, Safe Use of Radionuclides and Emergency Procedures.............................................................................................................................. 34 (ISA-14) Materials Security..................................................................................................... 36 (ISA-15) Waste Disposal......................................................................................................... 38 (ISA-16) Decommissioning of Group 1 and 2 Licenses.......................................................... 40 MATERIALS HEALTH PHYSICS LICENSE REVIEWER ON-THE-JOB ACTIVITIES................ 42 (OJT-1) Pre-Licensing Guidance............................................................................................. 43 (OJT-2) New License Reviews................................................................................................ 45 (OJT-3) License Amendment Reviews.................................................................................... 47 (OJT-4) License Renewal Reviews......................................................................................... 49 (OJT-5) Change of Control Reviews....................................................................................... 51 (OJT-6) License Termination Reviews.................................................................................... 53 (OJT-7) Financial Assurance................................................................................................... 55

Issue Date: XX/XX/25 ii 1248 App A Materials Health Physics License Reviewer Qualification Signature Cards and Certification..... 57 Form 1: Materials Health Physics License Reviewer Qualification Equivalency Justification..... 60 : Revision History Table for IMC 1248, Appendix A............................................... 63 : Common Signature Authority Process................................................................... 1

Issue Date: XX/XX/25 1

1248 App A INTRODUCTION The U.S. Nuclear Regulatory Commission (NRC) Materials Health Physics License Reviewer (license reviewer) qualification program requires completion of a variety of activities designed to help you, the license reviewer candidate, learn information or practice skills important to independently performing this critical function. When you have completed the entire qualification process, you will have demonstrated each of the competencies that delineate a successful license reviewer. The role of a license reviewer is to implement NRC policy by determining if activities proposed in the license application can be performed safely and securely and in compliance with NRC regulations, using NRC guidance documents. The license reviewers role is not to set policy in the areas of health and safety or security. A license reviewer should refer policy questions to management and the program office.

The Atomic Energy Act of 1954, as amended, gave authority to perform materials license reviews to the Office of Nuclear Materials Safety and Safeguards (NMSS), and the NMSS Director delegated licensing authority to the NMSS staff. For many years, licensing was only performed by headquarters staff in NMSS. In a memorandum dated October 6, 1987, the NMSS Director and the Executive Director for Operations delegated authority for performing certain license reviews to the regional administrators (Agencywide Documents Access and Management System (ADAMS) Accession No. ML100830226). The regional administrators each redelegated authority for licensing to the directors of the regional divisions responsible for materials licensing, currently the Division of Radiological Safey and Security (DRSS), and specified their requirements for further redelegation to the DRSS staff. In implementing Appendix A to Inspection Manual Chapter (IMC) 1248 for license reviewers, care should be taken to comply with the regional administrators requirements as specified in the delegation of authority.

A competent license reviewer should:

a.

Understand the legal basis and the processes used for achieving the NRCs regulatory objectives.

b.

Acquire a fundamental understanding of the NRCs organizational structure, mission, goals, and objectives.

c.

Understand the basis for the authority of the agency.

d.

Understand the processes established to achieve the regulatory objectives.

e.

Master the techniques and skills needed to collect, analyze, and integrate information using a safety and security focus to develop a supportable regulatory conclusion.

f.

Have the personal and interpersonal skills to carry out assigned regulatory activities either individually or as a member of a team.

Issue Date: XX/XX/25 2

1248 App A PROGRAM ORGANIZATION The license reviewer qualification process develops your awareness of the role of the agency, your role and skill as a license reviewer, and your technical expertise for reviewing licensing actions for the purposes of protecting health and safety and security.

The final activity in the qualification process is to appear before a qualification board.

Successful completion of the qualification board examination validates your understanding of the role of the agency, NMSS programs, and your role as a license reviewer. Upon successful completion of all the activities in the qualification journal, including the qualification board, you become eligible to receive the Materials Health Physics License Reviewer Qualification Certification.

QUALIFICATION JOURNAL ORGANIZATION The qualification journal identifies the training courses, the Individual Study Activities (ISAs), and On-The-Job Training (OJT) activities you must complete. Document your progress on the signature cards and certifications as you move through the qualification process. The journal also contains a form to document the justification for accepting equivalent training or experience as a way to meet license reviewer qualification requirements. The signature cards, certification, and equivalency justification pages form the permanent record of completing the license reviewer qualification program.

Upon certification, the qualification memorandum will be placed into the ADAMS and the qualification information entered into the Talent Management System (TMS) by sending a request to TrainingSupport.Resource@nrc.gov. The request to the TMS support group shall include the persons name, qualification achieved, date qualified and the Accession number of the ADAMS entry. The certification document that was placed into ADAMS and recorded in TMS shall serve as proof of inspector qualification. The license reviewer may retain their qualification signature and equivalency card(s).

Your immediate supervisor should assign a qualified license reviewer to assist you. This person would serve as a resource and mentor by answering any questions or providing guidance as you work to complete this qualification journal.

REQUIRED TRAINING COURSES The required training courses are the minimum courses you should take to complete the Materials Health Physics License Reviewer Qualification. The following courses may be taken in any order:

Medical Uses of Radiation Self-Study Course (H317S)

Industrial Radiography (H305)

Inspection Procedures (G108)

Licensing Practices and Procedures (G109)

Transportation of Radioactive Materials Self-Study Course (H308S)

Issue Date: XX/XX/25 3

1248 App A NRC Materials Control, Security Systems & Principles (S201)

Fundamental Health Physics (H122S)

Fundamental Health Physics Labs (H122L)

Advanced Health Physics (H201)

Human Resources Learning & Development (HRLD) suggests candidates take the Advanced Health Physics (H201) course as one of their last required courses. The H201 course builds on the different concepts taught in the other training courses. HRLD believes that candidates will have a better understanding of health physics concepts and technology if they take the H201 later in the qualification program.

Immediate supervisors have the authority to waive any of the training based on the experience of the candidate seeking qualification as a license reviewer. Document the reason for the waiver on Form 1: Materials Health Physics License Reviewer Equivalency Justification. While your immediate supervisor may waive certain classes, your qualification still requires certification by your regional administrator, office director, or their designee.

SPECIALIZED TRAINING COURSES The specialized training classes listed below may be completed as part of your training but are not required for formal qualifications. Your immediate supervisor will determine the appropriate training courses you must take to complete the license reviewer qualification based on the types of licensing work you will be assigned. For example, your immediate supervisor may require you to complete the Safety Aspects of Well Logging course (H314) or the Irradiator Technology course (H315) or both (see Specialized Training Courses below) if your region has a significant number of these licensees.

Root Cause/Incident Investigation Workshop (G205)

Environmental Monitoring and Air Sampling for Radioactivity Course (H130S)

Environmental Monitoring and Air Sampling for Radioactivity Lab Course (H130L)

Respiratory Protection (H311S)

Internal Dosimetry Self-Study Course (H312S)

Well Logging (H314)

NOTE: Advanced Health Physics (H-201) is a challenging 4.5-day course. Prior to enrolling in this course, the NRC requires that the following courses be completed as prerequisites: Fundamental HP Self-Study Course (H-122S) and Fundamental Health Physics Labs (H-122L). The candidates resource or mentor and/or immediate supervisor should be able to help determine which courses, if any, the candidate should take before enrolling in the Advanced Health Physics (H-201) course.

Issue Date: XX/XX/25 4

1248 App A Irradiator Technology (H315)

Multi-Agency Radiation Survey and Site Investigation (MARSSIM Self-Study) (H121S)

Multi-Agency Radiation Survey and Assessment of Materials and Equipment (MARSSAME Self-Study) (H120S)

RESRAD Overview (H408)

Advanced RESRAD Training Workshop (H412)

MILDOS-Area Training Workshop (H413)

Visual Sampling Plan (H500)

Additional courses may be developed after the publication of this qualification journal.

Immediate supervisors may include these new specialized training courses in the qualification journals.

REFRESHER TRAINING Qualified license reviewers must maintain their qualification by completing 36 hours4.166667e-4 days <br />0.01 hours <br />5.952381e-5 weeks <br />1.3698e-5 months <br /> of refresher training in the established requalification triennial cycle. The beginning of each requalification cycle will be determined using the year the license reviewer completed their qualification and will begin in the next triennial cycle. The license reviewers immediate supervisor may grant a 6-month extension, if for good reason, the license reviewer was unable to complete the required refresher training within the limits of the requalification cycle.

Refresher training may consist of either health and safety or security topics. The qualified license reviewers immediate supervisor will determine the training courses the license reviewer needs and will coordinate with HRLD staff, as necessary, to obtain the needed training.

Additionally, the supervisor can consult with HRLD staff to help identify specific courses that the staff member can take for refresher training. Examples of training that may be considered include: Health Physics Topics (H401), NRC technical training courses, external training courses, attending lectures, developing presentations on subjects related to health and safety or security, directed self-study courses, or other training approved by the qualified license reviewers immediate supervisor.

It is important to note that only taking a single course may not be enough refresher training.

Completing the refresher training will depend on the number of hours that the qualified staff member has completed.

Before taking refresher training, license reviewers should receive approval from their immediate supervisor to confirm that the training will be credited as refresher training. The immediate supervisor should take into consideration the objectives of the training and determine whether the training will be beneficial to the license reviewer. When considering a self-study style of training, the immediate supervisor should determine whether the training is appropriately structured. If the immediate supervisor is unsure if the self-study training is appropriate, he or she may want to consult with HRTD staff for its analysis of the training.

Issue Date: XX/XX/25 5

1248 App A To receive credit and track the number of hours needed for refresher training for training offered outside of the NRC training catalog, the license reviewer and immediate supervisor should provide the course details (title of training, number of hours, etc.) to either his or her division training coordinator or the appropriate HRTD staff. If there is any concern about the content of the training, HRTD management and the qualified license reviewers management will resolve the concern.

MATERIALS HEALTH PHYSICS LICENSE REVIEWER COMPETENCIES The training and qualification program detailed in this qualification journal ensures that every license reviewer acquires competency in three general areas:

Area 1: Understand the legal basis and the regulatory processes for achieving the NRCs regulatory objectives by:

Acquiring a fundamental understanding of the NRCs organizational structure, mission, goals, and objectives (Regulatory Framework)

Understanding the basis for the authority of the agency (Regulatory Framework)

Understanding the processes established to achieve the regulatory objectives (Regulatory Framework)

Area 2: Acquire the techniques and skills needed to collect, analyze, and integrate information using a safety and security focus to develop a supportable regulatory conclusion by:

Independently gathering information through objective review, observation, and open communication (Inspection)

Evaluating licensing information by conducting an objective review (Licensing Activities)

Determining acceptability of information by comparing to established criteria (Inspection and Licensing Activities)

NOTE: License reviewers may retake a course they had taken previously. An immediate supervisor should consider whether it would be beneficial for the license reviewer to retake the course. An immediate supervisor should consider whether there have been changes in technology, regulations, or if the course has changed considerably since the last time the license reviewer took the course before allowing a course to be retaken as refresher training. If the immediate supervisor allows the license reviewer to retake the course, the license reviewer must complete and pass the exam, if the course has one, to receive credit for the course.

Issue Date: XX/XX/25 6

1248 App A Objectively analyzing and integrating information using a safety focus to identify the appropriate regulatory conclusion and regulatory response (Enforcement)

Area 3: Have the personal and interpersonal skills to carry out assigned regulatory activities either individually or as a member of a team by:

Expressing ideas or thoughts clearly, carefully listening, and speaking and writing with appropriate safety focus and context (Communication)

Working collaboratively with others toward common objectives (Teamwork)

Working independently, exercising judgment, and exhibiting flexibility in the completion of activities including during difficult or challenging situations (Self-Management)

Using technology to locate, gather, manipulate, and share information (Information Technology)

Issue Date: XX/XX/25 7

1248 App A MATERIALS HEALTH PHYSICS LICENSE REVIEWER INDIVIDUAL STUDY ACTIVITY The ISAs direct and focus your efforts as you review documents and perform technical training assignments important to the performance of your job. Each activity begins with a purpose statement informing you of why the activity is important and how it relates to the license reviewer function. The evaluation criteria identify what you are expected to achieve upon completing the activity. The evaluation criteria are listed up front so that you can review them first. Use the evaluation criteria to help you focus on what is most important. The tasks outline the things you must do to successfully address the evaluation criteria. Each ISA includes an estimate for the level of effort needed to complete all the activities. These are estimates are to help guide the staff.

The following general guidance applies as you complete the various study activities:

Complete all assigned parts of each activity.

Your immediate supervisor will act as a resource as you complete each activity. Your immediate supervisor also may designate other qualified license reviewers to work with you as you complete the various activities. Discuss any questions you may have about the content of anything you read with your immediate supervisor or mentor.

You are responsible for keeping track of the tasks you have completed. Be sure to complete all the tasks in each activity before meeting with your immediate supervisor for an evaluation.

Issue Date: XX/XX/25 8

1248 App A TOPIC:

(ISA1) Web-Based Licensing PURPOSE:

The Web-Based Licensing (WBL) System is a web-based software solution developed to manage and support the information and processes related to the licensing of radioactive materials. The purpose of this activity is to familiarize you with the WBL System by learning how to conduct a search, properly enter data, and generate a license.

COMPETENCY AREA:

REGULATORY FRAMEWORK LEVEL OF EFFORT:

12 Hours

REFERENCES:

1. NRC Public Website for Integrated Source Management Portfolio (ISMP): https://www.nrc.gov/security/byproduct/ismp.html
2. WBL website: https://wbl.nrc-gateway.gov/saml/sp/profile/post/acs
3. Web-Based Licensing User Guide (located on the WBL website)

EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of WBL and how it is used by successfully completing the following:

1. Describe the purpose of WBL and how the agency uses it.
2. Describe the different methods used to search WBL, including how to create a custom search.
3. Describe the information that needs to be entered in the Information, Program Code, Locations, Materials, Authorized Use, Conditions, Authorized Users, ARSO, and FinAssurance tabs.
4. Explain the Compare and Sync function on the History tab and how its used.
5. Describe how to generate a license from WBL.
6. Explain each Milestone and when they should be used.

TASKS:

1. Obtain access to the Web-Based Licensing system (credentialing) by contacting the WBL Helpdesk.
2. Review the search function and learn how to conduct searches using the licensees name, license number, docket number, control number, and how to create a custom search for multiple licenses

Issue Date: XX/XX/25 9

1248 App A (for example, how to use WBL to determine all the licenses in one geographical area.)

3. Review the licensing module, the inspection module, the reciprocity module, and the general license tracking system, to get familiar with the information and features of the system. Make sure you do not edit or alter any record (do not press save) that is not assigned to you in support of your developmental activities.
4. Review the WBL User Guide to gain an understanding of the types and format of information that needs to be entered into WBL to generate a license.
5. Meet with a qualified license reviewer to discuss how to complete searches and to gain an understanding of the information that needs to be entered into WBL for a licensing action.
6. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA1.

Issue Date: XX/XX/25 10 1248 App A TOPIC:

(ISA2) The Role of Agreement States in Radioactive Materials Regulation Under Section 274 PURPOSE:

The purpose of this activity is to familiarize you with the role of the Agreement States in the regulatory framework for radioactive material.

During this activity, you will review Section 274 of the Atomic Energy Act and familiarize yourself with areas under which Agreement States assume regulatory responsibility for byproduct, source, and special nuclear material and the NRC discontinues its authority.

This activity will introduce you to the oversight program that the NRC retains over the Agreement State programs and familiarize you with the regional or office points of contact that have been established for Agreement State agencies. This activity also will introduce you to the National Materials Program (NMP) and the role of the two State organizations, the Organization of Agreement States (OAS) and the Conference of Radiation Control Program Directors (CRCPD), and their relationship with the NRC.

COMPETENCY AREA:

REGULATORY FRAMEWORK LEVEL OF EFFORT:

6 Hours

REFERENCES:

1. Section 274 of the Atomic Energy Act of 1954, as amended (Note:

The Energy Policy Act of 2005, Public Law 109-58, Title VI, section 651(e)(2), 119 Stat. 807 (2005), revised the definition of byproduct material in Section 274b)

2. Title 10 of the Code of Federal Regulations (10 CFR) Part 150, Exemptions and Continued Regulatory Authority in Agreement States and in Offshore Waters under Section 274 (Note the unique requirements for uranium recovery programs in Agreement States)
3. Agreement State Program Policy Statement (82 FR 48535; October 18, 2017)
4. Management Directive (MD) 5.6, Integrated Materials Performance Evaluation Program (IMPEP)
5. NMSS Procedure SA10, Joint Oversight of the National Materials Program
6. NMSS Procedure SA100, Implementation of the Integrated

Issue Date: XX/XX/25 11 1248 App A Materials Performance Evaluation Program (IMPEP)

7. National Materials Program (NMP) website https://www.nrc.gov/materials/nmp.html
8. Organization of Agreement States website, http://www.agreementstates.org/
9. Conference of Radiation Control Program Directors, Inc., website, http://www.crcpd.org/

EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the Agreement State program and the NRCs oversight of the program by successfully doing the following:

1. Discuss the purpose of Section 274 of the Atomic Energy Act of 1954, as amended.
2. Discuss the different categories of materials that Agreement States can assume regulatory authority over under a 274b agreement between the NRC and the State. Discuss the differences between a limited Agreement and a full Agreement.
3. Discuss the NRCs oversight program conducted under IMPEP.
4. Describe the common and noncommon performance indicators used to evaluate Agreement State and NRC performance.
5. Describe what the finding of Adequacy and Compatibility means for an Agreement State.
6. Discuss the relationship and roles within the National Materials Program (NMP):
a. The NRC and the individual Agreement States
b. The NRC and OAS
c. The NRC and CRCPD
d. OAS and CRCPD
7. Identify the Regional State Agreement Officers and describe their responsibilities. Describe the organizations within NMSS with responsibility for the Agreement State program oversight and interactions.

TASKS:

1. Review Section 274 of the Atomic Energy Act of 1954, as amended, and be able to explain its purpose.
2. Review SA10, Joint Oversight of the National Materials Program,

Issue Date: XX/XX/25 12 1248 App A to learn about the Agreement States and their role in the regulation of radioactive materials.

3. Review MD 5.6, Integrated Materials Performance Evaluation Program (IMPEP) and SA100, Implementation of the Integrated Materials Performance Evaluation Program (IMPEP) to gain an understanding of the IMPEP program.
4. Meet with the Regional State Agreement Officer for your Region or a member of the Agreement State Program Branch, NMSS, to discuss their roles and interactions with Agreement States.
5. Review and discuss the evaluation criteria with your immediate supervisor.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA2.

Issue Date: XX/XX/25 13 1248 App A TOPIC:

(ISA3) Reciprocity PURPOSE:

The purpose of this activity is to familiarize you with the process for granting reciprocity to Agreement State licensees for proposed licensed activities at temporary job sites located in Non-Agreement States, areas of exclusive Federal jurisdiction, or offshore waters.

COMPETENCY AREA:

REGULATORY FRAMEWORK COMMUNICATIONS LEVEL OF EFFORT:

6 Hours

REFERENCES:

1. 10 CFR 150.20, Recognition of Agreement State Licenses
2. NUREG1556, Volume 19, Consolidated Guidance about Materials Licenses: Guidance for Agreement State Licensees about NRC Form 241 Report of Proposed Activities in Non-Agreement States, Areas of Exclusive Federal Jurisdiction, or Offshore Waters and Guidance for NRC Licensees Proposing to Work in Agreement State Jurisdiction (Reciprocity)
3. IMC 0610, Nuclear Material Safety and Safeguards Inspection Reports EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of reciprocity by successfully doing the following:

1. Identify the regulations that allow an Agreement State licensee to conduct licensed activities in Non-Agreement States, areas of exclusive Federal jurisdiction, or offshore waters.
2. Describe areas of exclusive Federal jurisdiction. Describe an area that may not be under exclusive Federal jurisdiction. Describe who would make this determination.
3. Discuss the regulatory and license requirements the Agreement State licensee is under while working in the Non-Agreement State, area of exclusive Federal jurisdiction, or offshore waters.
4. Describe why the filing of reciprocity is important to safety and security.
5. Explain the NRCs process for granting reciprocity to Agreement State licensees wishing to conduct licensed activities at temporary

Issue Date: XX/XX/25 14 1248 App A job sites located in Non-Agreement States, areas of exclusive Federal jurisdiction, and offshore waters.

TASKS:

1. Review NUREG1556, Volume 19, Consolidated Guidance about Materials Licenses: Guidance for Agreement State Licensees about NRC Form 241 Report of Proposed Activities in Non-Agreement States, Areas of Exclusive Federal Jurisdiction, or Offshore Waters and Guidance for NRC Licensees Proposing to Work in Agreement State Jurisdiction (Reciprocity) to gain an understanding of reciprocity.
2. Meet with an individual experienced in your Regions processing of reciprocity requests and discuss the process. Discuss cases in which reciprocity was not given and why. Discuss the types of licensed activities conducted under reciprocity.
3. Review and discuss the evaluation criteria with your immediate supervisor.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA3.

Issue Date: XX/XX/25 15 1248 App A TOPIC:

(ISA4) Overview of 10 CFR Parts 30 through 39 PURPOSE:

The purpose of this activity is to acquaint you with the regulations that specify the requirements for byproduct materials licensed by the NRC. This ISA will help you to understand the regulations and become familiar with specific requirements in the regulations.

COMPETENCY AREA:

REGULATORY FRAMEWORK LEVEL OF EFFORT:

30 Hours

REFERENCES:

1. Paper or electronic copy of 10 CFR Parts 30-39 EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your general understanding of 10 CFR Parts 30 through 39 and why these regulations are important. Identify with your immediate supervisor what parts of the regulations you should focus on during your review. These may be in addition to what is listed below:

1. State the purpose of 10 CFR Parts 30, 31, 32, 33, 34, 35, 36, 37 and 39.
2. Given a specific subject, identify which section in 10 CFR discusses the requirements for that subject.
3. Discuss the parts of the regulations identified as the focus area for your discipline.
4. Discuss the difference between specific license of limited scope, specific license of broad scope, general license, and persons exempt from licensing.

TASKS:

1. Review 10 CFR Part 30 for a general understanding of the following:
a. Exemptions (30.11-30.22)
b. Licenses (30.31, 30.34, 30.41)
c. Reporting requirements (30.50)
d. Records (30.51)
2. Review 10 CFR Part 31 for a general understanding of the following:
a. Restrictions and limitations of licenses
b. Types, quantities, and forms of material
3. Review 10 CFR Part 32 for a general understanding of the following:
a. Types of licenses issued under this part.
b. Differences in the reporting and labeling requirements.

Issue Date: XX/XX/25 16 1248 App A

c. Sealed source and device registration
4. Review 10 CFR Part 33 for a general understanding of the following:
a. Types of licenses and how the category (Type A, B or C) is determined (33.11)
b. Differences in the requirements of each type of license (33.13, 33.14, 33.15)
c. Approval process for individuals using material under the license (33.17 (b), (c), (d))
5. Review 10 CFR Part 34 for a general understanding of the following:
a. Purpose (34.1)
b. Survey instrument requirement (34.25)
c. Inspection and maintenance of equipment (34.31)
d. Radiation safety requirements (34.41, 34.47, 34.49, 34.53)
e. Notification requirements (34.101)
6. Review 10 CFR Part 35 for a general understanding of the following:
a. Purpose (35.1)
b. Radiation protection programs (35.24)
c. Written directives (35.40-35.41)
d. General technical requirements (Subpart C)
e. Unsealed byproduct material - written directive not required (35.100 and 35.200)
f.

Unsealed byproduct material - written directive required (35.300)

g. Manual Brachytherapy (35.400)
h. Photon Emitting Remote Afterloader Units, Teletherapy Units, and Gamma Stereotactic Radiosurgery Units (Subpart H)
i.

Other medical uses (35.1000)

j.

Reports (Subpart M)

7. Review 10 CFR Part 36 for a general understanding of the following:
a. Purpose (36.1)
b. Access control (36.23)
c. Design requirements (36.39)
d. Personnel monitoring and radiation surveys (36.55, 36.57)
e. Inspection and maintenance (36.61)
f.

Attendance during operation (36.65)

g. Reports (36.83)
8. Review 10 CFR Part 37 for a general understanding of the following:
a. Purpose (37.1)

Issue Date: XX/XX/25 17 1248 App A

b. Access authorization program requirements (37.23, 37.25)
c. General security program requirements (37.43)
d. Requirements for mobile devices (37.53)
e. Reports (37.57, 37.81)
f.

Appendix A

9. Review 10 CFR Part 39 for a general understanding of the following:
a. Purpose (39.1)
b. Agreement with well owner or operator (39.15)
c. Radiation surveys (39.67)
d. Security, records, notifications (Subpart E)
10. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA4.

Issue Date: XX/XX/25 18 1248 App A TOPIC:

(ISA5) Overview of NUREG1556 PURPOSE:

The purpose of this activity is to familiarize you with the NUREG1556 Series. The NUREG documents are program-specific guidance designed to be used by applicants, licensees, and NRC staff.

Applicants and licensees use the NUREG volumes to prepare license applications, amendments, and other licensing actions. The NRC staff will use the NUREG volumes in its review of requests for licensing actions. In this ISA, you will become familiar with the different types of program-specific guidance available to licensees and NRC staff.

COMPETENCY AREA:

REGULATORY FRAMEWORK LICENSING ACTIVITIES LEVEL OF EFFORT:

8 Hours

REFERENCES:

1. NUREG1556 Series, Consolidated Guidance about Materials Licenses EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the NUREG1556 Series by successfully doing the following:

1. Describe the purpose of the NUREG1556 series and how it is used by applicants and license reviewers.
2. Identify the topics covered in NUREG1556 and where you can find them within each volume.
a. Locations where licensed materials will be used
b. Radioactive materials and how they will be used
c. Training and experience for Radiation Safety Officers (ROSs), Authorized Users, and individuals working in restricted areas
d. Facility descriptions
e. The radiation safety program, including audits, radiation monitoring equipment, occupational and public dose, procedures, maintenance, and transportation
f.

Waste management

g. License termination requirements
3. Describe the purpose of the of NUREG1556, Volume 20 and how license reviewers use it to complete licensing actions.

a) Processing license applications b) Requests for Additional Information (RAI) c) Creating a license d) Conducting licensing site visits e) Possession or storage only licenses f) Checklists g) Standard License Conditions

Issue Date: XX/XX/25 19 1248 App A

4. Describe the various types of checklists available in NUREG1556, Volume 20 and when they should be used.
5. Explain why standard license conditions are used, how a reviewer determines which should be used on a license and where they are located.

TASKS:

1. Locate on the NUREG1556 series on the NRCs webpage or obtain paper copies.
2. Coordinate with your supervisor to select one or more applicable NUREG1556 volume(s) to review. Gain an understanding of the basic layout and format for the guidance documents.
3. Review NUREG1556, Volume 20, Guidance About Administrative Licensing Procedures to gain an understanding of the guidance available to license reviewers.
4. Meet with a subject matter expert in the volume(s) that you reviewed.
5. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA5.

Issue Date: XX/XX/25 20 1248 App A TOPIC:

(ISA6) Radioactive Materials and Purposes for Which Licensed Material Will Be Used PURPOSE:

The purpose of this activity is to familiarize you with the types of radioactive materials used by NRC licensees, how they are used and the guidance available in NUREG1556 Series. In this ISA, you will become familiar with the different types of program-specific guidance available to licensees and NRC staff and the sealed source and device registry.

COMPETENCY AREA:

REGULATORY FRAMEWORK LICENSING ACTIVITIES LEVEL OF EFFORT:

20 Hours

REFERENCES:

1. NUREG1556 Series, Consolidated Guidance about Materials Licenses
2. Sealed Source and Device Registry EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of radioactive materials and purposes for which they are used by answering the following:

1. For the following programs that use sealed sources, describe the types of materials typically used, the chemical/physical form, quantities, depleted uranium when used as shielding, the purpose for how the materials will be used, and what should be included in an application:
a. Portable gauging devices
b. Fixed gauging devices
c. Industrial radiography devices
d. Well logging devices
e. Panoramic and self-shielded irradiators
f.

Research and development (including broadscope licensees)

g. Medical (brachytherapy, high dose-rate afterloader and gamma stereotactic surgery devices)
2. For the following programs that use unsealed radioactive materials, describe the types of materials typically used, quantities, the purpose for how the materials will be used and what should be included in an application:
a. Medical
b. Research and development (including broadscope licensees)
c. Manufacturing and Distribution
d. Radiopharmacy

Issue Date: XX/XX/25 21 1248 App A

e. Tracer and field studies
3. For programs authorizing the use of source and special nuclear materials less than critical mass, describe the radioactive materials, chemical/physical form, and quantities of materials.

TASKS:

1. Identify where on the NRCs public website you can locate the NUREG1556 Series.
2. Review sections 8.5 and 8.6 of the applicable NUREG1556 volumes and gain an understanding of the guidance for the various programs listed above.
3. Review several sealed source and device registrations, including ones for portable and fixed gauges, radiography devices, and medical uses to gain an understanding of the information included in the registration.
4. Meet with a subject matter expert to discuss the types of radioactive materials used by licensees.
5. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA6.

Issue Date: XX/XX/25 22 1248 App A TOPIC:

(ISA7) Radiation Safety Officer Training and Experience PURPOSE:

The purpose of this activity is to familiarize you with the training and experience for individuals named as RSOs on licenses. Included in the ISA is the training and experience for individuals who are named as members of Radiation Safety Committees (RSC). In this ISA, you will become familiar with the different program-specific guidance available to licensees and NRC staff.

COMPETENCY AREA:

REGULATORY FRAMEWORK LICENSING ACTIVITIES LEVEL OF EFFORT:

16 Hours

REFERENCES:

1. NUREG1556 Series, Consolidated Guidance about Materials Licenses
2. 10 CFR 30.33, General Requirements for Issuance of Specific Licenses
3. 10 CFR 35.50, Training for Radiation Safety Officers and Associate Radiation Safety Officer
4. 10 CFR 35.57, Training for experienced Radiation Safety Officer, teletherapy or medical physicist, authorized medical physicist, authorized user, nuclear pharmacist, and authorized nuclear pharmacist
5. 10 CFR 35.59, Recentness of Training
6. 10 CFR 40.32, General Requirements for Issuance of Specific Licenses
7. 10 CFR 70.22, Contents of Applications
8. NRC Form 313A (RSO), Radiation Safety Officer or Associate Radiation Safety Officer Training, Experience, and Preceptor Attestation EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the training and experience for RSOs and RSCs by answering the following:

1. For the following programs, describe the guidance on training and experience for individuals serving as RSOs:
a. Portable and fixed gauging
b. Industrial radiography
c. Well logging
d. Panoramic and self-shielded irradiators

Issue Date: XX/XX/25 23 1248 App A

e. Research and development (including broadscope licensees)
f.

Medical

g. Radiopharmacy
2. Describe when a delegation of authority for a new proposed RSO must be maintained and what information should be included.
3. Explain which licensees can name an Associate RSO, the guidance on training and experience information that shall be provided, and any other documentation that should be submitted in a license application.
4. Describe when a licensee must establish a radiation safety committee and the guidance on training and experience for committee members.

TASKS:

1. Identify where on the NRCs public website you can locate the NUREG1556 Series.
2. Review the guidance in Section 8 related to the training and experience for RSOs and RCSs in the applicable NUREG1556 volumes and gain an understanding of the guidance for the various programs listed above.
3. Review the regulations to gain an understand of the requirements related to naming a RSO on a license.
4. Meet with a subject matter expert to discuss the guidance for training of RSOs.
5. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA7.

Issue Date: XX/XX/25 24 1248 App A TOPIC:

(ISA8) Training and Experience for Authorized Users, Authorized Nuclear Pharmacist and Authorized Medical Physicist PURPOSE:

The purpose of this activity is to familiarize you with the training and experience individuals named as Authorized Users (AU), Authorized Nuclear Pharmacist (ANP) or Authorized Medical Physicist (AMP) on licenses. In this ISA, you will become familiar with the different program-specific guidance available to licensees and NRC staff.

COMPETENCY AREA:

REGULATORY FRAMEWORK LICENSING ACTIVITIES LEVEL OF EFFORT:

16 Hours

REFERENCES:

1. NUREG1556 Series, Consolidated Guidance about Materials Licenses
2. 10 CFR 30.33, General Requirements for Issuance of Specific Licenses
3. NRC Form 313A (AMP), Authorized Medical Physicist or Ophthalmic Physicist, Training, Experience, and Preceptor Attestation
4. NRC Form 313A (ANP), Authorized Nuclear Pharmacist Training, Experience, and Preceptor Attestation
5. NRC Form 313A (AUD), Authorized User Training, Experience, and Preceptor Attestation (for uses defined under 35.100, 35.200, and 35.500)
6. NRC Form 313A (AUS), Authorized User Training, Experience, and Preceptor Attestation (for uses defined under 35.400 and 35.600)
7. NRC Form 313A (AUT), Authorized User Training, Experience, and Preceptor Attestation (for uses defined under 35.300)
8. 10 CFR 40.32, General Requirements for Issuance of Specific Licenses
9. 10 CFR 70.22, Contents of Applications EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the training and experience for AUs, ANPs and AMPs by answering the following:

1. For the following programs, describe the guidance on training and experience for individuals serving as AUs:
a. Portable and fixed gauges

Issue Date: XX/XX/25 25 1248 App A

b. Industrial radiography
c. Well logging
d. Panoramic and self-shielded irradiators
e. Research and development (including broadscope licensees)
f.

Medical

g. Radiopharmacy
2. Describe the required training and experience for an individual serving as an ANP.
3. Describe the required training and experience for an individual serving as an AMP.

TASKS:

1. Identify where on the NRCs public website you can locate the NUREG1556 Series.
2. Review the guidance in Section 8 of the applicable NUREG1556 volumes to gain an understanding of the guidance on training and experience for AUs for the various programs listed above, and ANPs and AMPs.
3. Review the regulations to gain an understanding of the requirements related to training for AUs, ANPs and AMPs.
4. Meet with a subject matter expert to discuss the guidance on training for AUs, ANPs and AMPs.
5. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA8.

Issue Date: XX/XX/25 26 1248 App A TOPIC:

(ISA9) Facilities and Equipment PURPOSE:

The purpose of this activity is to familiarize you with the information that should be submitted by licensees and applicants related to their facilities and equipment, and the guidance available in NUREG1556 Series. In this ISA, you will become familiar with the different types of program-specific guidance available to licensees and NRC staff.

COMPETENCY AREA:

REGULATORY FRAMEWORK LICENSING ACTIVITIES LEVEL OF EFFORT:

6 Hours

REFERENCES:

1. NUREG1556 Series, Consolidated Guidance about Materials Licenses
2. 10 CFR 20.1801, Security of stored material
3. 10 CFR 30.33, General requirements for issuance of specific licenses
4. 10 CFR 35.12, Application for license, amendment, or renewal EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of an applicant or licensees facilities and equipment (e.g.

facility diagrams) by answering the following:

1. For the following programs describe the guidance on the types of information needed and what information should be submitted in an application for the proposed facilities and equipment:
a. Portable gauging devices
b. Fixed gauging devices
c. Industrial radiography devices
d. Well logging devices
e. Panoramic and self-shielded irradiators
f.

Research and development (including broadscope licensees)

g. Medical
h. Radiopharmacy TASKS:
1. Identify where on the NRCs public website you can locate the NUREG1556 Series.
2. Review section 8.9 of the applicable NUREG-1556 volumes and gain an understanding of the guidance for the various programs listed above.
3. Meet with a subject matter expert on the guidance related to facilities and equipment.

Issue Date: XX/XX/25 27 1248 App A

4. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA-9.

Issue Date: XX/XX/25 28 1248 App A TOPIC:

(ISA-10) Radiation Safety Program - Program Audit and Materials Receipt and Accountability PURPOSE:

The purpose of this activity is to familiarize you with the requirements for conducting program audits and documentation of materials received and maintained under the license and the guidance available in NUREG-1556 Series. In this ISA, you will become familiar with the different types of program-specific guidance available to licensees and NRC staff.

COMPETENCY AREA:

REGULATORY FRAMEWORK LICENSING ACTIVITIES LEVEL OF EFFORT:

6 Hours

REFERENCES:

1. NUREG-1556 Series, Consolidated Guidance about Materials Licenses
2. 10 CFR 20.1101, Radiation protection programs
3. 10 CFR 20.2102, Records of radiation protection programs
4. 10 CFR 30.51, Records EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the requirements for conducting program audits and documentation of materials received and maintained under the license by answering the following:

1. For the following programs describe the requirements for conducting program audits and documentation of materials received and maintained under the license and what should be submitted in an application:
a. Portable and fixed gauges
b. Industrial radiography
c. Well logging
d. Panoramic and self-shielded irradiators
e. Research and development (including broadscope licensees)
f.

Medical

g. Radiopharmacy TASKS:
1. Identify where on the NRCs public website you can locate the NUREG-1556 Series.
2. Review the sections of the applicable NUREG-1556 volumes related to program audits and material receipt and accountability to gain an understanding of the guidance for the various programs listed above.

Issue Date: XX/XX/25 29 1248 App A

3. Meet with a subject matter expert to gain understanding of the requirements for conducting audits and documentation of materials received and maintained under the license.
4. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA-10.

Issue Date: XX/XX/25 30 1248 App A TOPIC:

(ISA-11) Radiation Safety Program - Leak Testing, Radiation Monitoring Equipment and Surveys PURPOSE:

The purpose of this activity is to familiarize you with the requirements for leak testing of sealed sources, radiation monitoring equipment and conducting surveys and the guidance available in NUREG-1556 Series. In this ISA, you will become familiar with the different types of program-specific guidance available to licensees and NRC staff.

COMPETENCY AREA:

REGULATORY FRAMEWORK LICENSING ACTIVITIES LEVEL OF EFFORT:

6 Hours

REFERENCES:

1. NUREG-1556 Series, Consolidated Guidance about Materials Licenses
2. 10 CFR 20.1501, General
3. 10 CFR 20.2103, Records of surveys
4. 10 CFR 30.50, Reporting requirements
5. 10 CFR 30.53, Tests EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the requirements for leak testing of sealed sources, radiation monitoring equipment and conducting surveys by answering the following:

1. For programs that authorize the use of sealed sources, describe the requirements for conducting leak testing and what should be included in an application for the following:
a. Applicants who will use leak testing kits and/or utilize a licensed organization for sample analysis
b. Applicants requesting to conduct their own leak testing programs
2. For the following programs describe the requirements for radiation monitoring equipment and conducting surveys, including what should be submitted in an application:
a. Portable and fixed gauges
b. Industrial radiography
c. Well logging
d. Panoramic and self-shielded irradiators
e. Research and development (including broadscope licensees)
f.

Medical

g. Radiopharmacy

Issue Date: XX/XX/25 31 1248 App A TASKS:

1. Identify where on the NRCs public website you can locate the NUREG-1556 Series.
2. Review the sections of the applicable NUREG-1556 volumes related to leak testing of sealed sources, radiation monitoring equipment and conducting surveys to gain an understanding of the guidance for the various programs listed above.
3. Review several sealed source and device registrations, including ones for portable and fixed gauges, radiography devices, and medical uses to gain an understanding of the leak testing information included in the registration.
4. Meet with a subject matter expert to gain understanding of the requirements for leak testing of sealed sources, radiation monitoring equipment and conducting surveys.
5. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA-11.

Issue Date: XX/XX/25 32 1248 App A TOPIC:

(ISA-12) Radiation Safety Program - Occupational and Public Dose PURPOSE:

The purpose of this activity is to familiarize you with the requirements related to occupational and public dose and the guidance available in NUREG-1556 Series. In this ISA, you will become familiar with the different types of program-specific guidance available to licensees and NRC staff.

COMPETENCY AREA:

REGULATORY FRAMEWORK LICENSING ACTIVITIES LEVEL OF EFFORT:

6 Hours

REFERENCES:

1. NUREG-1556 Series, Consolidated Guidance about Materials Licenses
2. 10 CFR 20.1201, Occupational dose limits for adults
3. 10 CFR 20.1301, Dose limits for individual members of the public
4. 10 CFR 20.2106, Records of individual monitoring results
5. 10 CFR 20.2107, Records of dose to individual members of the public EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the requirements for monitoring both occupational and public dose by answering the following:

1. For the following programs describe the requirements for occupational dose monitoring, including what should be submitted in an application:
a. Portable and fixed gauges
b. Industrial radiography
c. Well logging
d. Panoramic and self-shielded irradiators
e. Research and development (including broadscope licensees)
f.

Medical

g. Radiopharmacy
2. Describe the NRC Forms that should be used to document occupational doses.
3. Describe the accepted methodologies for determining doses to members of the public from licensed activities. Explain who evaluates these determinations and what, if any, documentation should be provided in the application.

Issue Date: XX/XX/25 33 1248 App A TASKS:

1. Identify where on the NRCs public website you can locate the NUREG-1556 Series.
2. Review the sections of the applicable NUREG-1556 volumes related to occupational and public dose to gain an understanding of the guidance for the various programs listed above.
3. Meet with a subject matter expert to gain understanding of the licensing requirements for occupational and public dose.
4. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA-12.

Issue Date: XX/XX/25 34 1248 App A TOPIC:

(ISA-13) Radiation Safety Program - Operating, Safe Use of Radionuclides and Emergency Procedures PURPOSE:

The purpose of this activity is to familiarize you with the operating, safe use of radionuclides and emergency procedures and the guidance available in NUREG-1556 Series. In this ISA, you will become familiar with the different types of program-specific guidance available to licensees and NRC staff and the sealed source and device registry.

COMPETENCY AREA:

REGULATORY FRAMEWORK LICENSING ACTIVITIES LEVEL OF EFFORT:

12 Hours

REFERENCES:

1. NUREG-1556 Series, Consolidated Guidance about Materials Licenses
2. 10 CFR 20.1906, Procedures for receiving and opening packages
3. 10 CFR 30.32, Application for specific licenses
4. 10 CFR 35.12, Applications for license, amendment, or renewal EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of guidance on operating, safe use of radionuclides and emergency procedures and what applicants should provide in an application by answering the following:

1. For the following programs describe the guidance available and what should be included in an application regarding safe use and operating procedures:
a. Portable and fixed gauges
b. Industrial radiography
c. Well logging
d. Panoramic and self-shielded irradiators
e. Research and development (including broadscope licensees)
f.

Medical

g. Radiopharmacy
2. For the following programs describe the guidance available and what should be included in an application regarding security and emergency procedures:
a. Portable and fixed gauges
b. Industrial radiography
c. Well logging
d. Panoramic and self-shielded irradiators
e. Research and development (including broadscope licensees)

Issue Date: XX/XX/25 35 1248 App A

f.

Medical

g. Radiopharmacy TASKS:
1. Identify where on the NRCs public website you can locate the NUREG-1556 Series.
2. Review the sections related to operating, safe use of radionuclides and emergency procedures of the applicable NUREG-1556 volumes and gain an understanding of the guidance for the various programs listed above.
3. Meet with a subject matter expert in the volume(s) that you reviewed.
4. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA-13.

Issue Date: XX/XX/25 36 1248 App A TOPIC:

(ISA-14) Materials Security PURPOSE:

The purpose of this activity is to familiarize you with the security requirements imposed on certain licensees. This ISA will not make you a security expert, but it will provide you with a good understanding of the security requirements the NRC has in place. This activity also will require training on the appropriate handling of sensitive information and information protection.

COMPETENCY AREA:

LICENSING ACTIVITIES REGULATORY FRAMEWORK LEVEL OF EFFORT:

6 Hours

REFERENCES:

1. Memo - Request for Implementation of the Risk-Significant Radioactive Material Checklist and Guidance dated June 30, 2017 (ML17115A168)
2. 10 CFR 20.1801, Security of Stored Material
3. 10 CFR 20.1802, Control of Material Not in Storage
4. 10 CFR 30.34(i), Security Requirements for Portable Gauges
5. 10 CFR Part 37, Physical Protection of Category 1 and Category 2 Quantities of Radioactive Material
6. 10 CFR Part 73, Physical Protection of Plants and Materials
7. NUREG-2155, Implementation Guidance for 10 CFR Part 37, Physical Protection of Category 1 and Category 2 Quantities of Radioactive Material
8. NUREG-2166, Physical Security Best Practices for the Protection of Risk-Significant Radioactive Material
9. MD 12.6, NRC Controlled Unclassified Information Program EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of materials security and the different types of security requirements placed on various different types of licensees by successfully answering the following:

1. Discuss the proper handling of safeguards information and other types of security information, including how to safely store and transmit documents.

Issue Date: XX/XX/25 37 1248 App A

2. What are the requirements in 10 CFR 20.1801, Security of Stored Material, 10 CFR 20.1802, Control of Material Not in Storage, and 10 CFR 30.34(i), Security Requirements for Portable Gauges.
3. Describe the types of materials that require implementation of 10 CFR Part 37, Physical Protection of Category 1 and Category 2 Quantities of Radioactive Material.
4. Discuss the security requirements in 10 CFR Part 37, Physical Protection of Category 1 and Category 2 Quantities of Radioactive Material.
5. Describe how the NRC uses Risk-Significant Radioactive Materials (RSRM) Checklist and describe when it must be completed.

TASKS:

1. Complete the Information Security (INFOSEC) Awareness course and the Classified Information Awareness Training in TMS.
2. Review the regulations to gain an understanding of how licensees ensure radioactive materials remain secure.
3. Gain access to the IC Toolbox (password protected) at https://scp.nrc.gov/controls.html
4. Review the memo Request for Implementation of the Risk-Significant Radioactive Material Checklist and Guidance dated June 30, 2017 (ML17115A168) and gain an understanding of when the checklist needs to be completed and what information must be included.
5. Meet with a subject matter expert to gain understanding of the requirements for security requirements for radioactive materials.
6. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA-14.

Issue Date: XX/XX/25 38 1248 App A TOPIC:

(ISA-15) Waste Disposal PURPOSE:

The purpose of this activity is to familiarize you with various waste disposal methods and the guidance available in NUREG 1556. In this ISA, you will become familiar with the different types of program-specific guidance available to licensees and NRC staff.

COMPETENCY AREA:

LICENSING ACTIVITIES LEVEL OF EFFORT:

6 Hours

REFERENCES:

1. 10 CFR Part 20, Standards for Protection Against Radiation
2. 10 CFR Part 30, Rules of General Applicability to Domestic Licensing of Byproduct Material
3. Policy and Guidance Directive FC 8421, Incineration by Materials Licensees
4. NUREG-1241, Licensing of Alternative Methods of Disposal of Low-Level Radioactive Waste
5. NUREG-1556, Volumes 121, Consolidated Guidance about Materials Licenses EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the guidance on waste disposal and the information that applicants should provide in an application by answering the following:

1. Discuss the different waste disposal methods a licensee could request, and the potential risks and safety impacts associated with each method:
a. Transfer to an authorized recipient
b. Decay in storage
c. Release to sanitary sewer
d. Incineration
e. Compaction
f.

Disposal of Specific Waste as if It Were Not Radioactive

2. Describe the information a licensee or applicant would need to provide for each method of waste disposal listed above.

TASKS:

1. Review 10 CFR Parts 20.2001-20.2008 to gain an understanding of the regulatory requirements for the various methods of waste disposal.

Issue Date: XX/XX/25 39 1248 App A

2. Review the waste disposal section in several different volumes of NUREG-1556, including program areas that authorize both sealed and unsealed materials, to become familiar with the guidance.
3. Meet with a subject matter expert to gain understanding of the various waste disposal methods.
4. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA-15.

Issue Date: XX/XX/25 40 1248 App A TOPIC:

(ISA-16) Decommissioning of Group 1 and 2 Licenses PURPOSE:

The purpose of this activity is to familiarize you with the guidance for licensees decommissioning their facilities and make sure you understand that the Materials Health Physics License Reviewer qualification limits you to performing decommissioning reviews for only Group 1 and 2 facilities. Decommissioning of Group 3 though Group 7 facilities require qualification as a Decommissioning Project Manager/Technical Reviewer.

COMPETENCY AREA:

LICENSING ACTIVITIES LEVEL OF EFFORT:

8 Hours

REFERENCES:

1. 10 CFR Part 30, Rules of General Applicability to Domestic Licensing of Byproduct Material
2. 10 CFR Part 40, Domestic Licensing of Source Material
3. 10 CFR Part 70, Domestic Licensing of Special Nuclear Material
4. 10 CFR Part 51, Environmental Protection Regulations for Domestic Licensing and Related Regulatory Functions
5. NUREG-1757, Volumes 1, Consolidated Decommissioning Guidance: Decommissioning Process for Materials Licenses
6. NUREG-1556, Volumes 121, Consolidated Guidance about Materials Licenses EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the guidance on decommissioning requests and the information that licensees should provide in an application by answering the following:

1. Explain the purpose of NRC Form 314 and the information that licensees must provide.
2. Describe the decommissioning timeliness rules and what the regulations require of licensees.
3. Discuss the differences between decommissioning Groups 1-7 and who can review each group.
4. For a Group 1 licensed facility, describe the guidance on what information licensee should submit to the NRC when decommissioning.

Issue Date: XX/XX/25 41 1248 App A

5. For a Group 2 licensed facility, describe the guidance on what information licensee should submit to the NRC when decommissioning.
6. Explain how the National Environmental Policy Act can affect decommissioning licensing actions. When can a site qualify for a categorical exclusion and when must an environmental assessment be completed?

TASKS:

1. Review NUREG-1757, Volume 1, Consolidated Decommissioning Guidance: Decommissioning Process for Materials Licenses, to gain an understanding of the decommissioning licensing process and to learn about the decommissioning groups.
2. Review the license termination section in several volumes of NUREG 1556, including those that authorized sealed and unsealed radioactive materials, to gain an understanding of the guidance.
3. Meet with a subject matter expert to gain understanding of the guidance for licensees decommissioning their facilities.
4. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item ISA-16.

Issue Date: XX/XX/25 42 1248 App A MATERIALS HEALTH PHYSICS LICENSE REVIEWER ON-THE-JOB ACTIVITIES The Appendix A on-the-job training (OJT) activities require you to perform license reviews, as assigned by your immediate supervisor, under the supervision of qualified materials license reviewers. Like the ISAs, each OJT activity tells you why the activity is important and what you are expected to complete successfully during the activity. The OJT activities should be assigned to the reviewer to align with one of the core qualification signature authorities described in Attachment 1. Under the common signature authority process, staff will focus on learning the licensing process and gain an understanding of a specific area of review. At the completion of qualification program, the staff member will have the experience sufficient to receive signature authority in that program area.

Your immediate supervisor has the authority to waive any of the OJT modules by completing Form 1: Materials Health Physics License Reviewer Equivalency Justification, found at the end of this qualification journal.

THE FOLLOWING GENERAL GUIDANCE APPLIES AS YOU COMPLETE THE VARIOUS ON-THE-JOB ACTIVITIES:

Complete all parts of each activity.

Your immediate supervisor, qualified license reviewer, or qualified inspector will act as a resource as you complete each activity. Discuss any questions you may have about how a task must be done or how the guidance is to be applied. Your immediate supervisor will also designate other qualified license reviewers to work with you as you complete the various activities.

You are responsible for keeping track of the tasks you have completed. Be sure that you have completed all aspects of an OJT activity before you meet with your immediate supervisor, qualified license reviewer, or qualified inspector for evaluation.

Issue Date: XX/XX/25 43 1248 App A TOPIC:

(OJT-1) Pre-Licensing Guidance PURPOSE:

The purpose of this activity is to familiarize you with the NRCs pre-licensing process and with the use of the Pre-Licensing Guidance. As a license reviewer, you may on occasion be called upon to perform a pre-licensing visit to an applicants facility to confirm the legitimacy of the applicant and their planned activities.

COMPETENCY AREA:

LICENSING ACTIVITIES LEVEL OF EFFORT:

Note: The objective of this activity is to make sure that you have experience in licensing activities. The time needed to complete the tasks will depend on your individual proficiency. There are no set number of pre-licensing site visits you must complete. You must complete pre-licensing site visits until such time as you can address the evaluation criteria to the satisfaction of your supervisor, or the person designated to be your resource for this activity.

REFERENCES:

1. NRCs most current Pre-Licensing Guidance
2. Government Accountability Office (GAO) Report, Nuclear Security: Actions Taken by NRC to Strengthen Its Licensing Process for Sealed Radioactive Sources Are Not Effective, https://www.gao.gov/products/gao-071038t EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the NRC licensing process and demonstrate your ability to implement the Pre-Licensing Guidance by answering the following:

1. Discuss the GAOs report on nuclear security and the lessons learned.
2. Explain the purpose of the Pre-Licensing Guidance and when it should be used.
3. Describe when the Additional Screening Criteria are used and the purpose.
4. Explain the purpose of a Pre-Licensing Site Visit, including when one would be conducted, and the types of information gathered during the visit.
5. Describe when a Technical Assistance Request may be needed and the process for requesting additional support.

TASKS:

1. Review the GAO report to gain an understanding of the lessons learned and why the Pre-Licensing Guidance is such an important

Issue Date: XX/XX/25 44 1248 App A component to the security of radioactive materials.

2. Review and become familiar with the NRC Pre-Licensing Guidance, including how to determine if an applicant is a known entity and where to obtain information needed for the Additional Screening Criteria.
3. As assigned by your immediate supervisor, perform a new license review with an experienced license reviewer and use the Pre-Licensing Guidance to determine if a Basis for Confidence exists, including a pre-licensing site visit.
4. Review and understand the criteria for when and how to request technical assistance from NMSS related to the Pre-Licensing Guidance.
5. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item OJT-1.

Issue Date: XX/XX/25 45 1248 App A TOPIC:

(OJT-2) New License Reviews PURPOSE:

The purpose of this activity is to provide you with the skills needed to perform reviews of new license applications.

COMPETENCY AREA:

LICENSING ACTIVITIES LEVEL OF EFFORT:

Note: The objective of this activity is to make sure that you have experience in licensing activities. The time needed to complete the tasks will depend on your individual proficiency. There is no set number of licensing actions you must complete. You must participate in licensing actions until such time as you can address the evaluation criteria to the satisfaction of your supervisor, or the person designated to be your resource for this activity.

REFERENCES:

1. 10 CFR Part 30, Rules of General Applicability to Domestic Licensing of Byproduct Material
2. 10 CFR Part 37, Physical Protection of Category 1 and Category 2 Quantities of Radioactive Material
3. 10 CFR Part 71, Packaging and Transportation of Radioactive Material
4. NUREG-1556, Volume 20, Consolidated Guidance about Materials Licenses: Program-Specific Guidance about Portable Gauge Licenses
5. NUREG-1556, Volumes 121, Consolidated Guidance about Materials Licenses EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the NRC licensing process and demonstrate your ability to review new license applications and submit requests for additional information:

1. Describe the licensing actions completed, including any deficiencies that required additional information from the applicant or unique licensing requests.
2. Discuss the security requirements for licenses and when they must be implemented.
3. Discuss the forms that must be completed for all new licensing actions.
4. Describe the process for determining if an applicant is a known

Issue Date: XX/XX/25 46 1248 App A entity and the criteria for when a pre-licensing site visit must be completed.

TASKS:

1. As assigned by your immediate supervisor, and under the supervision of a qualified reviewer, complete licensing actions with a focus on those program codes under the core and/or discretionary signature authority.
2. For each licensing request assigned to you, use the appropriate NUREG-1556 Volume to assist you in your license review. Identify any information where the applicant did not provide an adequate response.
3. For any additional information needed to complete the review, work with a qualified license reviewer to develop a Request for Additional Information (RAI).
4. After completing the review of the request, including all responses to RAIs, draft the license in WBL, create the cover letter transmitting the license and complete any checklists that may need to be included.
5. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your immediate supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item OJT-2.

Issue Date: XX/XX/25 47 1248 App A TOPIC:

(OJT-3) License Amendment Reviews PURPOSE:

The purpose of this activity is to provide you with the skills needed to perform reviews of applications to amend licenses.

COMPETENCY AREA:

LICENSING ACTIVITIES LEVEL OF EFFORT:

Note: The objective of this activity is to make sure that you have experience in licensing activities. The time needed to complete the tasks will depend on your individual proficiency. There is no set number of licensing actions you must complete. You must participate in licensing actions until such time as you can address the evaluation criteria to the satisfaction of your supervisor, or the person designated to be your resource for this activity.

REFERENCES:

1. 10 CFR Part 30, Rules of General Applicability to Domestic Licensing of Byproduct Material
2. 10 CFR Part 37, Physical Protection of Category 1 and Category 2 Quantities of Radioactive Material
3. 10 CFR Part 71, Packaging and Transportation of Radioactive Material
4. NUREG-1556, Volume 20, Consolidated Guidance about Materials Licenses: Program-Specific Guidance about Portable Gauge Licenses
5. NUREG-1556, Volumes 121, Consolidated Guidance about Materials Licenses EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the NRC licensing process and demonstrate your ability to review license amendment requests and submit requests for additional information:

1. Describe the licensing actions completed, including any deficiencies that required additional information from the applicant or unique licensing requests. Be able to describe the information needed to make the following amendments, if applicable:
a. Increase or decrease the possession limit on a license
b. Changing a radiation safety officer
c. Adding a new authorized user
d. Adding or removing a new location of use
2. Discuss any requests for additional information completed and the applicants response.

Issue Date: XX/XX/25 48 1248 App A

3. Discuss any forms that must be completed when reviewing license amendment requests.

TASKS:

1. As assigned by your immediate supervisor, and under the supervision of a qualified reviewer, complete licensing actions with a focus on those program codes under the core and/or discretionary signature authority.
2. For each licensing request assigned to you, use the appropriate NUREG-1556 Volume to assist you in your license review. Identify any information where the applicant did not provide an adequate response.
3. For any additional information needed to complete the review, work with a qualified license review to develop a RAI.
4. After completing the review of the request, including all responses to RAIs, draft the license in WBL, create the cover letter transmitting the license and complete any checklists that may need to be included.
5. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your immediate supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item OJT-3.

Issue Date: XX/XX/25 49 1248 App A TOPIC:

(OJT-4) License Renewal Reviews PURPOSE:

The purpose of this activity is to provide you with the skills needed to perform reviews of license renewal applications.

COMPETENCY AREA:

LICENSING ACTIVITIES LEVEL OF EFFORT:

Note: The objective of this activity is to make sure that you have experience in licensing activities. The time needed to complete the tasks will depend on your individual proficiency. There is no set number of licensing actions you must complete. You must participate in licensing actions until such time as you can address the evaluation criteria to the satisfaction of your supervisor, or the person designated to be your resource for this activity.

REFERENCES:

1. 10 CFR Part 30, Rules of General Applicability to Domestic Licensing of Byproduct Material
2. 10 CFR Part 37, Physical Protection of Category 1 and Category 2 Quantities of Radioactive Material
3. 10 CFR Part 71, Packaging and Transportation of Radioactive Material
4. NUREG-1556, Volume 20, Consolidated Guidance about Materials Licenses: Program-Specific Guidance about Portable Gauge Licenses
5. NUREG-1556, Volumes 121, Consolidated Guidance about Materials Licenses EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the NRC licensing process and demonstrate your ability to review license renewal applications and submit requests for additional information:

1. Describe the licensing actions completed, including any deficiencies that required additional information from the applicant or unique licensing requests.
2. Discuss any requests for additional information completed and the applicants response.
3. Discuss the forms that must be completed for all license renewal actions and how they are documented.
4. Describe the process for determining license renewal term and what

Issue Date: XX/XX/25 50 1248 App A the requirements are when a shorter term is used.

TASKS:

1. As assigned by your immediate supervisor, and under the supervision of a qualified reviewer, complete licensing actions with a focus on those program codes under the core and/or discretionary signature authority.
2. For each licensing request assigned to you, use the appropriate NUREG-1556 Volume to assist you in your license review. Identify any information where the applicant did not provide an adequate response.
3. For any additional information needed to complete the review, work with a qualified license review to develop a RAI.
4. After completing the review of the request, including all responses to RAIs, draft the license in WBL, create the cover letter transmitting the license and complete any checklists that may need to be included.
5. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your immediate supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item OJT-4.

Issue Date: XX/XX/25 51 1248 App A TOPIC:

(OJT-5) Change of Control Reviews PURPOSE:

The purpose of this activity is to provide you with the skills needed to perform reviews of notification of a change of control.

COMPETENCY AREA:

LICENSING ACTIVITIES LEVEL OF EFFORT:

Note: The objective of this activity is to make sure that you have experience in licensing activities. The time needed to complete the tasks will depend on your individual proficiency. There is no set number of licensing actions you must complete. You must participate in licensing actions until such time as you can address the evaluation criteria to the satisfaction of your supervisor, or the person designated to be your resource for this activity.

REFERENCES:

1. 10 CFR Part 30, Rules of General Applicability to Domestic Licensing of Byproduct Material
2. NUREG-1556, Volumes 15, Consolidated Guidance about Materials Licenses: Guidance About Changes of Control and About Bankruptcy Involving Byproduct, Source, or Special Nuclear Materials Licenses EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the NRC licensing process and demonstrate your ability to review notifications of a change of control:

1. Describe how the NRC defines change of control and explain who determines if a change of control has occurred.
2. Describe the process for reviewing change of control requests, including the requirement to publicly post the request to the NRC public webpage.
3. Describe the licensing actions completed, including any deficiencies that required additional information from the applicant or unique requests.
4. Discuss the pre-licensing guidance and when it needs to be incorporated for change of control notifications.

TASKS:

1. As assigned by your immediate supervisor, and under the supervision of a qualified reviewer, complete reviews of notifications of a change of control.
2. For each notification assigned to you, use NUREG-1556 Volume 15 to assist you in your license review. Identify any information where the applicant did not provide an adequate response.

Issue Date: XX/XX/25 52 1248 App A

3. For any additional information needed to complete the review, work with a qualified license review to develop a RAI.
4. After completing the review of the request, including all responses to RAIs, draft the safety evaluation report and the cover letter and complete any checklists that may need to be included. If needed, draft a license amendment using WBL.
5. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your immediate supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item OJT-5.

Issue Date: XX/XX/25 53 1248 App A TOPIC:

(OJT-6) License Termination Reviews PURPOSE:

The purpose of this activity is to provide you with the skills needed to perform reviews of applications for license termination.

COMPETENCY AREA:

LICENSING ACTIVITIES LEVEL OF EFFORT:

Note: The objective of this activity is to make sure that you have experience in licensing activities. The time needed to complete the tasks will depend on your individual proficiency. There is no set number of licensing actions you must complete. You must participate in licensing actions until such time as you can address the evaluation criteria to the satisfaction of your supervisor, or the person designated to be your resource for this activity.

REFERENCES:

1. 10 CFR Part 30, Rules of General Applicability to Domestic Licensing of Byproduct Material
2. NUREG-1556, Volume 20, Consolidated Guidance about Materials Licenses: Program-Specific Guidance about Portable Gauge Licenses
3. NUREG-1556, Volumes 121, Consolidated Guidance about Materials Licenses
4. NUREG-1757, Volumes 1, Consolidated Decommissioning Guidance: Decommissioning Process for Materials Licenses EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of the NRC licensing process and demonstrate your ability to review license termination requests and submit requests for additional information:

1. Describe the licensing actions completed, including any deficiencies that required additional information from the applicant or unique licensing requests. Be able to describe the information needed to terminate a license, including the following:
a. Disposition of radioactive material
b. Survey results (if they are required)
2. Discuss the differences between decommissioning Groups 1-7 and who can review each group.
3. Discuss any requests for additional information completed and the applicants response.
4. Discuss any forms that must be completed when reviewing license

Issue Date: XX/XX/25 54 1248 App A termination amendment requests.

TASKS:

1. As assigned by your immediate supervisor, and under the supervision of a qualified reviewer, complete licensing actions with a focus on those program codes under the core and/or discretionary signature authority.
2. For each licensing request assigned to you, use the appropriate NUREG-1556 Volume to assist you in your license review. Identify any information where the applicant did not provide an adequate response.
3. For any additional information needed to complete the review, work with a qualified license review to develop a RAI.
4. After completing the review of the request, including all responses to RAIs, draft the license in WBL, create the cover letter transmitting the license and complete any checklists that may need to be included.
5. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your immediate supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item OJT-6.

Issue Date: XX/XX/25 55 1248 App A TOPIC:

(OJT-7) Financial Assurance PURPOSE:

The purpose of this activity is to familiarize you with the procedures, guidance, and activities applicable to approving material license financial assurance and handling documents.

COMPETENCY AREA:

REGULATORY FRAMEWORK LEVEL OF EFFORT:

20 Hours

REFERENCES:

1. 10 CFR 30.35, Financial Assurance and Recordkeeping for Decommissioning
2. 10 CFR 40.36, Financial Assurance and Recordkeeping for Decommissioning
3. 10 CFR 70.25, Financial Assurance and Recordkeeping for Decommissioning
4. NUREG-1757, Volume 3, Consolidated Decommissioning Guidance: Financial Assurance, Recordkeeping, and Timeliness
5. MD 8.12, Decommissioning Financial Assurance Instrument Security Program EVALUATION CRITERIA:

Upon completion of this activity, you will be asked to demonstrate your understanding of financial assurance requirements and what an applicant of licensee must submit by successfully doing the following:

1. Describe the purpose of financial assurance and how a license reviewer can determine when its required by a licensee or applicant.
2. Describe the difference between the prescribed dollar amount and a Decommissioning Funding Plan. What possession limits would require one over the other?
3. Describe the components of the Decommissioning Funding Plan.

How often is a licensees Decommissioning Funding Plan required to be updated?

4. Explain the purpose of a licensees Certification of Financial Assurance? When does this document need to be revised?
5. Describe the types of financial assurance instruments that are

Issue Date: XX/XX/25 56 1248 App A acceptable to the NRC. Explain the purpose and which instrument types require a Standby Trust Agreement.

6. Explain the requirements for submitting updates or revisions to the financial assurance instruments.
7. Describe the NRCs storage and handling criteria for original financial instruments.

TASKS:

1. Review 10 CFR 30.35, Financial Assurance and Recordkeeping for Decommissioning and NUREG-1757, Volume 3, Consolidated Decommissioning Guidance: Financial Assurance, Recordkeeping, and Timeliness to gain an understanding the requirements for financial assurance, including the documentation that needs to be provided to the NRC.
2. As assigned by your immediate supervisor, review financial assurance licensing actions. Actions should include a Decommissioning Funding Plan, a certified amount, an action with a Statement of Intent, an action with a letter of credit, and an action with a self or parent guarantee.
3. Review an annual test for licensee that has an approved self or parent company guarantee. What actions would need to be taken if a licensee cannot meet the test requirements?
4. Review MD 8.12, Decommissioning Financial Assurance Instrument Security Program to gain an understanding of the storage and handling requirements for financial assurance documents
5. Discuss with the Financial Assurance Instrument Custodian the process of storage and handling of original financial assurance instruments.
6. Meet with your immediate supervisor or the person designated to be your resource for this activity to discuss the items listed in the evaluation criteria section.

DOCUMENTATION:

Obtain your supervisor or designees signature in the line item for Qualification Journal Certification Signature Card Item OJT-7.

Issue Date: XX/XX/25 57 1248 App A Materials Health Physics License Reviewer Qualification Signature Cards and Certification Employee Name:

Employee Initials/Date Immediate Supervisor Signature/Date A. Required Training (title and course number)

Training: Medical Uses of Radiation Self-Study Course (H-317S)

Training: Industrial Radiography (H-305)

Training: Inspection Procedures (G-108)

Training: Licensing Practices and Procedures (G-109)

Training: Transportation of Radioactive Materials Self-Study Course (H-308S)

Training: NRC Materials Control, Security Systems & Principles (S-201)

Training: Fundamental Health Physics (H-122S)

Training: Fundamental Health Physics Labs (H-122L)

Training: Advanced Health Physics (H-201)

B. Specialized Training (title and course number)

Training: Root Cause/Incident Investigation Workshop (G-205)

Training: Environmental Monitoring and Air Sampling for Radioactivity Course (H-130S)

Training: Environmental Monitoring and Air Sampling for Radioactivity Lab Course (H-130L)

Training: Respiratory Protection (H-311S)

Training: Internal Dosimetry Self-Study (H-312S)

Training: Well Logging (H-314)

Training: Irradiator Technology (H-315)

Training: Multi-Agency Radiation Survey and Site Investigation (MARSSIM Self-Study) (H-121S)

Training: Multi-Agency Radiation Survey and Assessment of Materials and Equipment (MARSSAME Self-Study) (H-120S)

Training: RESRAD Overview (H-408)

Training: Advanced RESRAD Training Workshop (H-412)

Training: MILDOS-Area Training Workshop (H-413)

Issue Date: XX/XX/25 58 1248 App A Employee Name:

Employee Initials/Date Immediate Supervisor Signature/Date Training: Visual Sampling Plan (H-500)

Training:

Training:

C. Individual Study Activities ISA-1 Web-Based Licensing ISA-2 The Role of Agreement States in Radioactive Materials Regulation Under Section 274 ISA-3 Reciprocity ISA-4 Overview of 10 CFR Parts 30 through 39 ISA-5 Overview of NUREG 1556 ISA-6 Radioactive Materials and Purposes for Which Licensed Material Will Be Used ISA-7 Radiation Safety Officer Training and Experience ISA-8 Training and Experience for Authorized Users, Authorized Nuclear Pharmacist and Authorized Medical Physicist ISA-9 Facilities and Equipment ISA-10 Radiation Safety Program - Program Audit and Materials Receipt and Accountability ISA-11 Radiation Safety Program - Leak Testing, Radiation Monitoring Equipment and Surveys ISA-12 Radiation Safety Program - Occupational and Public Dose ISA-13 Radiation Safety Program - Operating, Safe Use of Radionuclides and Emergency Procedures ISA-14 Materials Security ISA-15 Waste Disposal ISA-16 Decommissioning of Group 1 and 2 Licenses D. On-the-Job Training Activity OJT-1 Pre-Licensing Guidance OJT-2 New License Reviews OJT-3 License Amendment Reviews OJT-4 License Renewal Reviews OJT-5 Change of Control Reviews

Issue Date: XX/XX/25 59 1248 App A Employee Name:

Employee Initials/Date Immediate Supervisor Signature/Date OJT-6 License Termination Reviews OJT-7 Financial Assurance Supervisors Certification for Inspector Qualification Signature/Date This signature card and certification must be accompanied by the appropriate Form 1, Materials Health Physics License Reviewer Qualification Equivalency Justification, if applicable. (The electronic signature card is also acceptable.) Record completion in TMS by sending a request to TrainingSupportResource@nrc.gov.

Issue Date: XX/XX/25 60 1248 App A Form 1: Materials Health Physics License Reviewer Qualification Equivalency Justification Employee Name:

Identify Equivalent Training and Experience for which credit is being given:

A. Required Training (title and course number)

Training: Medical Uses of Radiation Self-Study Course (H-317S)

Training: Industrial Radiography (H-305)

Training: Inspection Procedures (G-108)

Training: Licensing Practices and Procedures (G-109)

Training: Transportation of Radioactive Materials (H-308)

Training: NRC Materials Control & Security Systems & Principles (S-201)

Training: Fundamental Health Physics (H-122S)

Training: Fundamental Health Physics Labs (H-122L)

Training: Advanced Health Physics (H-201)

B. Specialized Training (title and course number)

Training: Root Cause/Incident Investigation Workshop (G-205)

Training: Environmental Monitoring and Air Sampling for Radioactivity Course (H-130S)

Training: Environmental Monitoring and Air Sampling for Radioactivity Lab Course (H-130L)

Training: Respiratory Protection (H-311S)

Training: Internal Dosimetry Self-Study (H-312S)

Training: Well Logging (H-314)

Training: Irradiator Technology (H-315)

Training: Multi-Agency Radiation Survey and Site Investigation (MARSSIM Self-Study) (H-121)

Training: Multi-Agency Radiation Survey and Assessment of Materials and Equipment (MARSSAME Self-Study) (H-120)

Training: RESRAD Overview (H-408)

Training: AdvancedRESRAD Training Workshop (H-412)

Training: MILDOS-Area Training Workshop (H-413)

Issue Date: XX/XX/25 61 1248 App A Employee Name:

Identify Equivalent Training and Experience for which credit is being given:

Training:

Training:

C. Individual Study Activities ISA-1 Web-Based Licensing ISA-2 The Role of Agreement States in Radioactive Materials Regulation Under Section 274 ISA-3 Reciprocity ISA-4 Overview of 10 CFR Parts 30 through 39 ISA-5 Overview of NUREG 1556 ISA-6 Radioactive Materials and Purposes for Which Licensed Material Will Be Used ISA-7 Radiation Safety Officer Training and Experience ISA-8 Training and Experience for Authorized Users, Authorized Nuclear Pharmacist and Authorized Medical Physicist ISA-9 Facilities and Equipment ISA-10 Radiation Safety Program - Program Audit and Materials Receipt and Accountability ISA-11 Radiation Safety Program - Leak Testing, Radiation Monitoring Equipment and Surveys ISA-12 Radiation Safety Program -

Occupational and Public Dose ISA-13 Radiation Safety Program -

Operating, Safe Use of Radionuclides and Emergency Procedures ISA-14 Materials Security ISA-15 Waste Disposal ISA-16 Decommissioning of Group 1 and 2 Licenses D. On-the-Job Training Activity OJT-1 Pre-Licensing Guidance OJT-2 New License Reviews OJT-3 License Amendment Reviews OJT-4 License Renewal Reviews OJT-5 Change of Control Reviews OJT-6 License Termination Reviews

Issue Date: XX/XX/25 62 1248 App A Employee Name:

Identify Equivalent Training and Experience for which credit is being given:

OJT-7 Financial Assurance Supervisors Recommendation Signature/Date:

Division Directors Approval Signature/Date:

Issue Date: XX/XX/25 Att-1.1 1248 App A : Revision History Table for IMC 1248, Appendix A Commitment Tracking Number Accession Number Issue Date Change Notice Description of Change Description of Training Required and Completion Date Comment Resolution Accession Number N/A ML112350968 10/26/11 CN 11022 Revision history sheet added. Combined Appendix A1 with Appendix B1 and renamed as IMC 1246 Appendix E1. Added Training Requirements Section from Appendix A1 N/A ML112350982 N/A ML12240A131 04/19/13 CN 13011 Has been renamed from IMC 1246 App E01 to IMC 1248 App A. and was created to remove and separate FSMENMSS activities from IMC 1246 Appendix E1 NMSS manual chapter series.

The qualification journal was completely revised to accommodate this change and include specific FSMENMSS information (i.e. the security of radioactive materials).

N/A ML12254B095 N/A ML25XXXAXXX XX/XX/25 CN 25XX N/A

Issue Date: XX/XX/25 Att-2.1 1248 App A : Common Signature Authority Process Part of the qualification process for a license reviewer qualifying under IMC 1248, Appendix A involves obtaining signature authority to independently review licensing actions (new applications, amendments, renewals, and terminations). The immediate supervisor, in consultation with the mentor(s), will regularly evaluate the candidates licensing reviews (casework) under the supervision of a qualified reviewer and grant the signature authority for the program codes the qualifying individual has demonstrated competency.

The qualifying individual must be assigned and complete the necessary casework to obtain core signature authority before being evaluated by the qualification board. The supervisor may tailor the core signature authority by assigning one or two additional groupings called, discretionary signature authority, during the qualification period. Any groups in the core or discretionary signature authority grouping not completed during the qualification period will be assigned to be completed within a year of qualification, together with other post-qualification groups identified by the supervisor.

Post-qualification any program codes not covered in the core or discretionary signature authority groups are divided into the post-qualification signature authority groups. It is expected that the supervisor and the qualifying individual will implement a yearly plan which specifies the post-qualification signature authority to be achieved during that period. As the reviewer continues to gain signature authority, the supervisor and license reviewer will revise the yearly plan and continue to identify the post-qualification signature authority groups to be achieved.

Your Region may not have every category of program code. In cases where there is not a certain category of license or very limited numbers such that it may not be possible for the candidate to complete the qualification journal in a reasonable period of time, the immediate supervisor may decide whether the specific program code needs to be completed for the candidate to complete his or her qualification. Alternatively, an immediate supervisor can have a candidate conduct license reviews of previously completed casework. It is not necessary nor expected that each license reviewer obtains signature authority in all the groups or program codes. However, the supervisor must ensure it has the needed qualified staff, with the needed signature authorities, to process licensing casework in their organization.

Issue Date: XX/XX/25 Att-2.2 1248 App A Core Qualification Signature Authority (Required for all)

Same for all regions - reflects common licensing priorities (workload) for each region.

Portable and Fixed Gauges

[Core SA 1]

Medical -Limited Scope: Written Directive Required and NOT Required

[Core SA 2]

Discretionary Qualification Signature Authority (Add-on)

Designed to adjust the core qual signature authority to distinct regional workload needs. (Add 1 or 2 during qualification process).

Industrial Radiography

[Discretionary SA 1]

Mobile Medical [Discretionary SA 2]

High Dose Remote Afterloader [Discretionary SA 3]

Post Qual Signature Authority The rest of the program codes are grouped to facilitate signature authority after the formal qualification process.

Candidates will have a 1-year post qualification plan in place by the time it gets qualified. The plan needs to be updated at least every year.

Issue Date: XX/XX/25 Att-2.3 1248 App A Core Signature Authority Groups Candidate demonstrates proficiency by successfully completing at least 2 complex (new application, renewal, change of control, or amendment increasing scope) licensing actions of different program codes in each group.

Core Signature Authority Group 1: Fixed and Portable Gauging Devices 03120 Measuring Systems Fixed Gauges, 15 Locations 04414 Measuring Systems Fixed Gauges, 620 Locations 04415 Measuring Systems Fixed Gauges, More Than 20 Locations 03121 Measuring Systems Portable Gauges, 15 Locations 04416 Measuring Systems Portable Gauges, 620 Locations 04417 Measuring Systems Portable Gauges, More Than 20 Locations 03122 Measuring Systems Analytical Instruments, 15 Locations 04418 Measuring Systems Analytical Instruments, 620 Locations 04419 Measuring Systems Analytical Instruments, More Than 20 Locations 03123 Measuring Systems Gas Chromatographs, 15 Locations 04420 Measuring Systems Gas Chromatographs, 620 Locations 04421 Measuring Systems Gas Chromatographs, More Than 20 Locations 03124 Measuring Systems Other, 15 Locations 04422 Measuring Systems Other, 620 Locations 04423 Measuring Systems Other, More Than 20 Locations 03130 Inspection Systems, 15 Locations 04436 Inspection Systems, 620 Locations 04437 Inspection Systems - More Than 20 Locations 03140 Industrial Diagnostic Systems, 15 Locations 04438 Industrial Diagnostic Systems, 620 Locations 04439 Industrial Diagnostic Systems, More Than 20 Locations 03710 Civil Defense Core Signature Authority Group 2: Medical 02121 Medical Institution Written Directive Not Required, 15 Locations 04812 Medical Institution Written Directive Not Required, 620 Locations 04813 Medical Institution Written Directive Not Required, More Than 20 Locations 02201 Medical Private Practice Written Directive Not Required, 15 Locations 04816 Medical Private Practice Written Directive Not Required, 620 Locations 04817 Medical Private Practice Written Directive Not Required, More Than 20 Locations 02220 Mobile Nuclear Medicine Service Written Directive Not Required, 15 Locations 04820 Mobile Nuclear Medicine Service Written Directive Not Required 20 Locations 04821 Mobile Nuclear Medicine Service Written Directive Not Required, More Than 20 Locations Discretionary Signature Authority Suggest adding 1 group, or 2 depending on the individuals knowledge level, during the qualification process. The remaining should move to the 1-year plan after qualification.

Discretionary Signature Authority Group 1: Industrial Radiography Minimum of 2 complex licensing actions from the listed program codes.

Issue Date: XX/XX/25 Att-2.4 1248 App A 03310 Industrial Radiography Fixed Location, 15 Locations 04310 Industrial Radiography Fixed Location, 620 Locations 04311 Industrial Radiography Fixed Location, More Than 20 Locations 03320 Industrial Radiography Temporary Job Sites, 15 Locations 04312 Industrial Radiography Temporary Job Sites, 620 Locations 04313 Industrial Radiography Temporary Job Sites, More Than 20 Locations Discretionary Signature Authority Group 2: Medical Minimum of 2 complex licensing actions from the listed program codes.

02120 Medical Institution Written Directive Required, 15 Locations 04810 Medical Institution Written Directive Required, 620 Locations 04811 Medical Institution Written Directive Required, More Than 20 Locations 02200 Medical Private Practice Written Directive Required, 15 Locations 04814 Medical Private Practice Written Directive Required, 620 Locations 04815 Medical Private Practice Written Directive Required, More Than 20 Locations 02231 Mobile Medical Services Written Directive Required, 15 Locations 04824 Mobile Medical Services Written Directive Required, 620 Locations 04825 Mobile Medical Services Written Directive Required, More Than 20 Locations 02210 Eye Applicators Stronitium-90, 15 Locations 04818 Eye Applicators Stronitium-90, 620 Locations 04819 Eye Applicators Stronitium-90, More Than 20 Locations 22160 Pacemaker Byproduct and/or SNMMedical Institution 04828 Pacemaker Byproduct and/or SNMMedical Institution, 620 Locations 04829 Pacemaker Byproduct and/or SNMMedical Institution, More Than 20 Locations 22161 Pacemaker Byproduct and/or SNMIndividual Discretionary Signature Authority Group 3: High Dose Remote Afterloader Minimum of 2 complex licensing actions from the listed program codes.

02230 High Dose Rate Remote Afterloader (HDR,) 15 Locations 04822 High Dose Rate Remote Afterloader (HDR,) 620 Locations 04823 High Dose Rate Remote Afterloader (HDR,) More Than 20 Locations Additional Program Codes Included with Core Signature Authority Once the candidate is qualified with core signature authority, they automatically get signature authority for the following program codes. No action is necessary to be completed. Supervisor or mentor should discuss these situations with the candidate.

03800 By-Product Possession Only (Priority 3 Exception) 04430 Byproduct Material Possession Only - Permanent Shutdown, 620 Locations 04431 Byproduct Material Possession Only - Permanent Shutdown, More Than 20 Locations 03810 By-Product StandbyNo Operations (Priority 3 Exception) 04432 Byproduct Material Standby - No Operations, 620 Locations 04433 Byproduct Material Standby - No Operations, More Than 20 Locations 11800 Source Material Possession Only - Permanent Shutdown 11810 Source Material Standby - No Operations 23300 SNM Possession Only (Non-Fuel)-Permanent Shutdown 23310 SNM Standby (Non-Fuel) - No Operations

Issue Date: XX/XX/25 Att-2.5 1248 App A Post Qualification Signature Authority Groups Candidate and supervisor need to identify the post qualification signature authority group(s) to be covered during a specified period. Candidate will have a 1-year post qualification plan in place following completion of core training. The plan must be updated at least every year.

Candidate demonstrates proficiency by successfully completing at least 2 complex (new application, renewal, change of control, or amendment increasing scope) licensing actions of different program codes in each group.

Post Qualification: Expanded Medical Minimum of 2 complex licensing actions from the listed program codes, need to be from different program types.

02110 Medical Institution Broad, 15 Locations 04710 Medical Institution Broad, 620 Locations 04711 Medical Institution Broad, More Than 20 Locations 02240 Medical TherapyOther Emerging Technology, 15 Locations 04826 Medical TherapyOther Emerging Technology, 620 Locations 04827 Medical TherapyOther Emerging Technology, More Than 20 Locations 02300 Teletherapy, 15 Locations 04510 Teletherapy, 620 Locations 04511 Teletherapy, More Than 20 Locations 02310 Gamma Stereotactic Radiosurgery, 15 Locations 04512 Gamma Stereotactic Radiosurgery, 620 Locations 04513 Gamma Stereotactic Radiosurgery, More Than 20 Locations Post Qualification: Irradiators And Well Logging Minimum of 2 complex licensing actions from the listed program codes, need to be from different program types.

03110 Well Logging Byproduct and/or SNM Tracer & Sealed Sources 03111 Well Logging Byproduct and/or SNM Sealed Sources Only 03112 Well Logging Byproduct Only-Tracers Only 03113 Field Flooding Studies 03510 Irradiators Self-Shielded Less Than or Equal To 10,000 Curies 03511 Irradiators Other Less Than or Equal To 10,000 Curies 03520 Irradiators Self-Shielded Greater Than 10,000 Curies 03521 Irradiators Other Greater Than 10,000 Curies Post Qualification: Research And Development Minimum of 2 complex licensing actions from the listed program codes, need to be from different program types.

01120 Academic Type C Broad, 15 Locations 04622 Academic Type C Broad Multisite-Multiregional, 620 Locations 04623 Academic Type C Broad Multisite-Multiregional, More Than 20 Locations 03612 Research and Development Type C Broad, 15 Locations 04614 Research and Development Type C Broad, 620 Locations 04615 Research and Development Type C Broad, More Than 20 Locations 03620 Research and Development Other, 15 Locations

Issue Date: XX/XX/25 Att-2.6 1248 App A 03613 R&D Broad - Multisite-Multiregional, 15 Locations 04616 R&D Broad - Multisite-Multiregional, 620 Locations 04617 R&D Broad - Multisite-Multiregional, More Than 20 Locations 02400 Veterinary-Nonhuman Subjects, 15 Locations 04410 Veterinary - Nonhuman Subjects, 620 Locations 04411 Veterinary - Nonhuman Subjects, More Than 20 Locations 02410 In-Vitro Testing Laboratories, 15 Locations 04412 In-Vitro Testing Laboratories, 620 Locations 04413 In-Vitro Testing Laboratories, More Than 20 Locations 03614 Master Materials Licenses Post Qualification: Broadscope Research and Development Minimum of 2 complex licensing actions from the listed program codes, need to be from different program types.

01100 Academic Type A Broad, 15 Locations 04618 Academic Type A Broad -Multisite-Multiregional, 620 Locations 04619 Academic Type A Broad -Multisite-Multiregional, More Than 20 Locations 01110 Academic Type B Broad, 15 Locations 04620 Academic Type B Broad -Multisite-Multiregional, 620 Locations 04621 Academic Type B Broad -Multisite-Multiregional, More Than 20 Locations 03211 Manufacturing and Distribution Broad - Type A, 15 Locations 04010 Manufacturing and Distribution Broad - Type A, 620 Locations 04011 Manufacturing and Distribution Broad - Type A, More Than 20 Locations 03212 Manufacturing and Distribution Broad - Type B, 15 Locations 04012 Manufacturing and Distribution Broad - Type B, 620 Locations 04013 Manufacturing and Distribution Broad - Type B, More Than 20 Locations 03610 Research and Development Type A Broad, 15 Locations 04610 Research and Development Type A Broad, 620 Locations 04611 Research and Development Type A Broad, More Than 20 Locations 03611 Research and Development Type B Broad, 15 Locations 04612 Research and Development Type B Broad, 620 Locations 04613 Research and Development Type B Broad, More Than 20 Locations Post Qualification: Nuclear Pharmacy, Cyclotrons and Service Providers Minimum of 2 complex licensing actions from the listed program codes, need to be from different program types.

02500 Nuclear Pharmacies, 15 Locations 04210 Nuclear Pharmacies, 620 Locations 04211 Nuclear Pharmacies, More Than 20 Locations 03210 Radionuclide Production Using an Accelerator 02600 Production of Pet Radioactive Drugs-30.32(J) (Secondary Code) 03218 Nuclear Laundry 03219 Decontamination Services 03220 Leak Test Service Only, 15 Locations 04424 Leak Test Services Only, 620 Locations 04425 Leak Test Service Only, More Than 20 Locations 03221 Instrument Calibration Services Only - Source Less Than or Equal to 100 Curies, 15

Issue Date: XX/XX/25 Att-2.7 1248 App A Locations 04426 Instrument Calibration Services Only - Source Less Than or Equal to 100 Curies, 620 Locations 04427 Instrument Calibration Services Only - Source Less Than or Equal to 100 Curies, More Than 20 Locations 03222 Instrument Calibration Services Only - Source Greater Than or Equal to 100 Curies, 15 Locations 04428 Instrument Calibration Services Only - Source Greater Than or Equal to 100 Curies, 620 Locations 04429 Instrument Calibration Services Only - Source Greater Than or Equal to 100 Curies, More Than 20 Locations 03225 Other Services, Source Less Than or Equal to 100 Curies 03226 Other Services Greater Than 100 Curies Post Qualification: Manufacturing and Distribution Minimum of 2 complex licensing actions from the listed program codes, need to be from different program types.

02511 Medical Product Dist.-32.72Prepared Radiopharmaceuticals, 15 Locations 04212 Medical Product Distribution-32.72 Prepared Radiopharmaceuticals, 620 Locations 04213 Medical Product Distribution-32.72 Prepared Radiopharmaceuticals, More Than 20 Locations 02513 Med. Product Dist.-32.74-Sources & Devices 04214 Medical Product Distribution-32.74 Sources and Devices - 620 Locations 04215 Medical Product Distribution-32.74 Sources and Devices, More Than 20 Locations 03213 Manufacturing and Distribution Broad - Type C, 15 Locations 04014 Manufacturing and Distribution Broad - Type C, 620 Locations 04015 Manufacturing and Distribution Broad - Type C, More Than 20 Locations 03214 Manufacturing and Distribution Broad - Other, 15 Locations 04110 Manufacturing and Distribution Broad - Other, 620 Locations 04111 Manufacturing and Distribution Broad - Other, More Than 20 Locations 02700 Radium-226 Luminous Products & Sources Up To 10 Times 31.12(A) (4) & (5) 02711 Radium-226 Luminous Products & Sources Greater Than 10 Times 31.12(A) (4) & (5) 03215 Manufacture, Assembly, Disassembly, Repair Products Containing Radium-226, 15 Locations 04112 Manufacture, Assembly, Disassembly, Repair Products Containing Radium-226, 620 Locations 04113 Manufacture, Assembly, Disassembly, Repair Products Containing Radium-226, More Than 20 Locations 03240 General License Distribution - 32.51 03241 General License Distribution - 32.53 03242 General License Distribution - 32.57 03243 General License Distribution - 32.61 03244 General License Distribution - 32.71 22170 SNM General License Distribution (70.39) 22135 Power Sources with Byproduct Material - Manufacturing & Distribution 22136 Power Sources with SNM - Manufacturing & Distribution 04114 Power Sources with Byproduct Material - Manufacturing & Distribution, 620 Locations 04115 Power Sources with Byproduct Material - Manufacturing & Distribution, More Than 20 Locations

Issue Date: XX/XX/25 Att-2.8 1248 App A 22162 Pacemaker - Byproduct and/or SNM - Manufacturing & Distribution 04116 Pacemaker - Byproduct Material - Manufacturing & Distribution, 6-20 Locations 04117 Pacemaker - Byproduct Material - Manufacturing & Distribution, More Than 20 Locations Post Qualification: Various Program Codes Minimum of 2 complex licensing actions from the listed program codes, need to be from different program types.

03900 Decommissioning of By-Product Material Facilities 11900 Decommissioning of Source Material Facilities 22200 Decommissioning of Special Nuclear Material Facilities 03231 Waste Disposal (Burial) 03232 Waste Disposal Service Prepackaged Only 03233 Waste Disposal Service Incineration 03234 Waste Disposal Service Processing and/or Repackaging 03235 Incineration - Noncommercial (Secondary Code) 03236 Waste Treatment Service (Other than Compaction) 22130 Power Sources with Byproduct and/or SNM 22131 Power Sources with Special Nuclear Material 04434 Power Sources with Byproduct Material, 620 Locations 04435 Power Sources with Byproduct Material, More Than 20 Locations 11200 Source Material Other Less Than 150 Kilograms 11210 Source Material Shielding 11230 Source Material General License Distribution - 40.34 11231 Source Material General License Distribution - 40.54 11300 Source Material Other Greater Than 150 Kilograms 11700 Rare Earth Extraction and Processing 11710 Source Material Manufacturer/Distributor 11820 Source Material Removal as Contaminates from Water Treatment 11220 Source Material Military Munition - Indoor Testing 11221 Source Material Military Munition - Outdoor Testing 22110 SNM Plutonium - Unsealed, Less Than Critical Mass 22111 SNM, U-235 and/or U-233, Unsealed, Less Than Critical Mass 22120 SNM Plutonium - Sealed Neutron Sources Less Than 200 Grams 22140 SNM Plutonium - Sealed Sources in Devices 22150 SNM Plutonium - Sealed Sources Less Than Critical Mass 22151 SNM U-235 and/or U-233 Sealed Sources Less Than Critical Mass 22170 SNM General License Distribution (70.39) 25110 Transportation - Private Carriage

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