Pages that link to "10 CFR 35.27, Supervision"
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The following pages link to 10 CFR 35.27, Supervision:
Displayed 50 items.
- 10 CFR 35.27 (redirect page) (← links)
- 10 CFR 32.72 (← links)
- 10 CFR 35 (← links)
- Information Notice 2007-32, Out of Service Equipment Connected To In Service Process Line Results in Fissile Solution Spill at Fuel Cycle Facility (← links)
- Information Notice 2007-38, Ensuring Complete and Accurate Information in the Documentation of Training and Experience for Individuals Seeking Medical Authorization Under the Alternate Pathway (← links)
- Information Notice 2007-31, U.S. Food and Drug Administration Announcement Related to Sleep Disorder Drugs (← links)
- Information Notice 2007-25, Recommendations From the Advisory Committee on the Medical Use of Isotopes for Improved Compliance with 10 CFR 35.40 and 35.27 (← links)
- Information Notice 2002-23, Unauthorized Administration of Byproduct Material for Medical Use (← links)
- Information Notice 1985-70, Teletherapy Unit Full Calibration and Qualified Expert Requirements (10 CFR 35.23 and 10 CFR 35.24) (← links)
- Information Notice 2002-28, Appointment of Radiation Safety Officers and Authorized Users Under 10 CFR Part 35 (← links)
- Information Notice 2007-25, Recommendations from the Advisory Committee on the Medical Use of Isotopes for Improved Compliance with 10 CFR 35.40 and 35.27 (← links)
- ML18176A377 (← links)
- ML18099A350 (← links)
- ML17338A449 (← links)
- Information Notice 2008-10, Response to Indications of Potential Tampering Vandalism or Malicious Mischief (← links)
- NUREG-1556 Volume 13, Rev 2 - Consolidated Guidance About Materials Licenses - Program-Specific Guidance About Commercial Radiopharmacy Licenses - Final Report (← links)
- NUREG-1556 Volume 21, Rev. 1, Consolidated Guidance About Materials Licenses - Program-Specific Guidance About Possession Licenses for Production of Radioactive Material Using an Accelerator - Final Report. (← links)
- ML19106A367 (← links)
- ML19198A305 (← links)
- NUREG-1556 Volume 9, Rev. 3, Consolidated Guidance About Materials Licenses: Program-Specific Guidance About Medical Use Licenses Final Report (← links)
- ML19176A454 (← links)
- ML20043F492 (← links)
- ML20126E077 (← links)
- ML20261H504 (← links)
- ML20151Z047 (← links)
- ML20151S294 (← links)
- ML20196L402 (← links)
- ML20281A519 (← links)
- ML20239A086 (← links)
- ML20237B719 (← links)
- ML20249B895 (← links)
- ML20247E463 (← links)
- ML21272A165 (← links)
- ML21288A126 (← links)
- ML20210L239 (← links)
- ML20207E512 (← links)
- ML22012A067 (← links)
- ML21337A216 (← links)
- ML22021B576 (← links)
- ML22063A454 (← links)
- ML22334A269 (← links)
- ML22334A102 (← links)
- ML22322A157 (← links)
- ML23205A181 (← links)
- ML23240A718 (← links)
- ML23257A263 (← links)
- ML24023A297 (← links)
- ML24156A188 (← links)
- ML24156A187 (← links)
- ML24033A303 (← links)
- ML24200A183 (← links)
- ML24016A109 (← links)
- ML23325A190 (← links)
- 10 CFR 35 (← links)
- 10 CFR 35.1, Purpose and Scope (← links)
- 10 CFR 35.2, Definitions (← links)
- 10 CFR 35.5, Maintenance of Records (← links)
- 10 CFR 35.6, Provisions for the Protection of Human Research Subjects (← links)
- 10 CFR 35.7, Fda, Other Federal, and State Requirements (← links)
- 10 CFR 35.8, Information Collection Requirements: Omb Approval (← links)
- 10 CFR 35.10, Implementation (← links)
- 10 CFR 35.11, License Required (← links)
- 10 CFR 35.12, Application for License, Amendment, Or Renewal (← links)
- 10 CFR 35.13, License Amendments (← links)
- 10 CFR 35.14, Notifications (← links)
- 10 CFR 35.15, Exemptions Regarding Type a Specific Licenses of Broad Scope (← links)
- 10 CFR 35.18, License Issuance (← links)
- 10 CFR 35.19, Specific Exemptions (← links)
- 10 CFR 35.24, Authority and Responsibilities for the Radiation Protection Program (← links)
- 10 CFR 35.26, Radiation Protection Program Changes (← links)
- 10 CFR 35.40, Written Directives (← links)
- 10 CFR 35.41, Procedures for Administrations Requiring a Written Directive (← links)
- 10 CFR 35.49, Suppliers for Sealed Sources Or Devices for Medical Use (← links)
- 10 CFR 35.50, Training for Radiation Safety Officer (← links)
- 10 CFR 35.51, Training for an Authorized Medical Physicist (← links)
- 10 CFR 35.55, Training for an Authorized Nuclear Pharmacist (← links)
- 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 (← links)
- 10 CFR 35.59, Recentness of Training (← links)
- 10 CFR 35.60, Possession, Use, and Calibration of Instruments Used to Measure the Activity of Unsealed Byproduct Material (← links)
- 10 CFR 35.61, Calibration of Survey Instruments (← links)
- 10 CFR 35.63, Determination of Dosages of Unsealed Byproduct Material for Medical Use (← links)
- 10 CFR 35.65, Authorization for Calibration, Transmission, and Reference Sources (← links)
- 10 CFR 35.67, Requirements for Possession of Sealed Sources and Brachytherapy Sources (← links)
- 10 CFR 35.69, Labeling of Vials and Syringes (← links)
- 10 CFR 35.70, Surveys of Ambient Radiation Exposure Rate (← links)
- 10 CFR 35.75, Release of Individuals Containing Unsealed Byproduct Material Or Implants Containing Byproduct Material (← links)
- 10 CFR 35.80, Provision of Mobile Medical Service (← links)
- 10 CFR 35.92, Decay-In-Storage (← links)
- 10 CFR 35.100, Use of Unsealed Byproduct Material for Uptake, Dilution, and Excretion Studies for Which a Written Directive Is Not Required (← links)
- 10 CFR 35.190, Training for Uptake, Dilution, and Excretion Studies (← links)
- 10 CFR 35.200, Use of Unsealed Byproduct Material for Imaging and Localization Studies for Which a Written Directive Is Not Required (← links)
- 10 CFR 35.204, Permissible Molybdenum-99, Strontium-82, and Strontium-85 Concentrations (← links)
- 10 CFR 35.290, Training for Imaging and Localization Studies (← links)
- 10 CFR 35.300, Use of Unsealed Byproduct Material for Which a Written Directive Is Required (← links)
- 10 CFR 35.310, Safety Instruction (← links)
- 10 CFR 35.315, Safety Precautions (← links)
- 10 CFR 35.390, Training for Use of Unsealed Byproduct Material for Which a Written Directive Is Required (← links)
- 10 CFR 35.392, Training for the Oral Administration of Sodium Iodide I-131 Requiring a Written Directive In Quantities Less Than Or Equal to 1.22 Gigabecquerels (33 Millicuries) (← links)
- 10 CFR 35.394, Training for the Oral Administration of Sodium Iodide I-131 Requiring a Written Directive In Quantities Greater Than 1.22 Gigabecquerels (33 Millicuries) (← links)
- 10 CFR 35.400, Use of Sources for Manual Brachytherapy (← links)
- 10 CFR 35.404, Surveys After Source Implant and Removal (← links)
- 10 CFR 35.406, Brachytherapy Sources Accountability (← links)