ML20236Y616
| ML20236Y616 | |
| Person / Time | |
|---|---|
| Issue date: | 08/11/1998 |
| From: | Shelton B NRC OFFICE OF INFORMATION RESOURCES MANAGEMENT (IRM) |
| To: | |
| Shared Package | |
| ML20236Y609 | List: |
| References | |
| NUDOCS 9808120353 | |
| Download: ML20236Y616 (5) | |
Text
l:
I 'g
[7590-01-P) l U. S. NUCLEAR REGULATORY COMMISSION Documents Containing Reporting or Recordkeeping Requirements: Office of Management and Budget (OMB) Review AGENCY:
U. S. Nuclear Regulatory Commission (NRC)
ACTION:
Notice of the OMB review of information collection and solicitation of public comment.
SUMMARY
The NRC has recently submitted to OMB for review the following proposal for the collection ofinformation under the provisions of the Paperwork Reduction Act of 1995 (44 U.S.C. Chapter 35).
1.
Type of submission, new, revision, or extension: Revision 2.
The title of the information collection:
-10 CFR Part 35, Medical Use of Byproduct Material
- NRC Form 313 Application for Material License, and Supplemental Forms NRC Form 313A, Training and Experience, and NRC Form 313B, Preceptor Statement 3.
The form number if applicable: NRC Form 313,313A and 313B 9908120353 990811
?
~
2 4.
How often the collection is required: Reports of medical events; dose embryo / fetus or nursing child, or leaking sources are reportable on An organization desiring to become a certifying entity must tender an application upon intent.
- 5. Who will be required or asked to report:
Physicians and medicalinstitutions holding an NRC license authorizing the administration of byproduct m rediation therefrom to humans for medical use.
- 6. An estimate of the number of responses:
93,966 (26,850 NRC licensees, 67,116 Agreement State licensees). In addition,4 new organizations are expected to apply to become certifying entities and 35 will be required to submit modified procedures.
- 7. The estimated number of annual respondents:
1,902 NRC li ensees and 4,755 Agreement State licensees.
- 8. An estimate of the total number of hours needed annually to complete requirement or request:
Part 35: 877,807 hours0.00934 days <br />0.224 hours <br />0.00133 weeks <br />3.070635e-4 months <br /> (251,192 hours0.00222 days <br />0.0533 hours <br />3.174603e-4 weeks <br />7.3056e-5 months <br /> for NRC licensees,626,381 hours0.00441 days <br />0.106 hours <br />6.299603e-4 weeks <br />1.449705e-4 months <br /> for Agreement State licensees and 234 hours0.00271 days <br />0.065 hours <br />3.869048e-4 weeks <br />8.9037e-5 months <br /> f r
certifying organizations)(an average of 132 hours0.00153 days <br />0.0367 hours <br />2.18254e-4 weeks <br />5.0226e-5 months <br /> perlicensee). In addition there is a one-time burden of 2,956 hours0.0111 days <br />0.266 hours <br />0.00158 weeks <br />3.63758e-4 months <br /> for certifying organizations to m
new or modified procedures. NRC Form 313: 68 additional hours (48 hours5.555556e-4 days <br />0.0133 hours <br />7.936508e-5 weeks <br />1.8264e-5 months <br /> for NRC licensees and 20 hours2.314815e-4 days <br />0.00556 hours <br />3.306878e-5 weeks <br />7.61e-6 months <br /> for Agreement State licensees).
c.
3
- 9. An indication of whether Section 3507(d), Pub. L.104-13 applies: Applicable I
- 10. Abstract: 10 CFR Part 35, " Medical Use of Byproduct Material," is being restructured into a risk-informed performance-based regulation. The proposed rule contains mandatory requirements that apply to NRC licensees authorized to administer byproduct material or radiation therefrom to humans for medical use. In addition, requirements are being added for organizations desiring to be recognized by NRC as certifying organizations.
The information in the required reports and records is used by the NRC to ensure that public health and safety is protected, and that the possession and use of byproduct materialis in compliance with the license and regulatory requirements.
I l
Submit, by (insert date 30 days after publication in the Federal Reoister), comments that address the following questions:
1.
Is the proposed collection of information necessary for the NRC to properly perform its functions? Does the information have practical utility?
2.
Is the burden est' mate accurate?
3.
Is there a way to enhance the quality, utility, and clarity of the information to be i
collected?
t
E i
e.
1 4
4.
How can the burden of the information co;lection be minimized, including the use of automated collection techniques or other forms ofinformation technology?
A copy of the submittal may be viewed free of charge at the NRC Public Document Room 2120 L Street, NW (lower level), Washington, DC. The proposed rule indicated in 'The title of the information collection"is or has been published in the Federal Reaister within several days of the publication date of this Federal Register Notice. Instructions for accessing the electronic OMB clearance package for the rulemaking have been appended to the electronic rulemaking.
i Members of the public may access the electronic OMB clearance package by following the l
l directions for electronic access provided in the preamble to the titled rulemaking.
l Comments and questions should be directed to the OMB reviewer by (insert date 30 deys after i
i publication in the Federal Reaisterk Erik Godwin Office of Information and Regulatory Affairs (3150-0010, and -0120)
NEOB-10202 Office of Management and Budget Washington DC 20503 i
i l
f..
e 0
5 Comments can also be submitted by telephone at (202) 395-5084.
The NRC Clearance Officer is Brenda Jo. Shelton,301-415-7233.
Dated at Rockville, Maryland, this // day of b u/1998.
U For the Nuclear Regulatory Commission.
b seth St. Mary, Acting Clearance Officer Office of the ChiefInf tion Officer i
F i
k
.