NRC Form 313, Application for Material License, NRC Form 313A, Medical Use Training and Experience and Preceptor Attestation.

Forms and Documents

Document Name	Status
Form NRC-313 NRC Form 313, Application for Material License, NRC Form 313A, Medical use Training and Experience and Preceptor Attestation. Form	Modified
40-22 Proposed Rule SS revised 11-24-10.doc Supporting Statement A	2010-11-29

IC Document Collections

IC ID	Document Title	Status
33369	NRC Form 313, Application for Material License, NRC Form 313A, Medical use Training and Experience and Preceptor Attestation. Form	Modified

ICR Details

OMB Control No: 3150-0120	ICR Reference No: 201007-3150-010
Status: Historical Inactive	Previous ICR Reference No: 200810-3150-005
Agency/Subagency: NRC	Agency Tracking No:
Title: NRC Form 313, Application for Material License, NRC Form 313A, Medical Use Training and Experience and Preceptor Attestation.
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Comment filed on proposed rule and continue	Conclusion Date: 01/03/2011
	Date Received in OIRA: 08/12/2010
Terms of Clearance: In accordance with 5 CFR 1320, comment filed on proposed rule. Agency to address comments received at the final rule stage.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	03/31/2012	03/31/2012	05/31/2012
Responses	15,127	0	15,127
Time Burden (Hours)	65,224	0	65,224
Cost Burden (Dollars)	0	0	0

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Abstract: 10 CFR Parts 30, 40, 70, 170, and 171, Distribution of Source Material to Exempt Persons and to General Licensees and Revision of General License and Exemptions, PROPOSED RULE The NRC is proposing to amend its regulations in 10 CFR Part 40 to establish new requirements for distributors of source material to persons exempt from the regulations or for use under a general license in § 40.22. In addition, the Commission is also proposing to modify the existing possession and use requirements for § 40.22 general licensees to align the requirements with current health and safety standards. Finally, the Commission is proposing to revise, clarify, or delete certain exemptions in § 40.13(c) to make the exemptions more risk informed. Conforming changes would be made to 10 CFR Parts 30, 70, 170 and 171. These changes would affect manufacturers and distributors of products and materials containing source material and future users of some products used under exemptions from licensing and under the § 40.22 general license. Information collections would result from new requirements for certain persons initially distributing source material to obtain a specific license. These new specific licensees would be required to provide reports regarding their initial distributions of source material to the NRC and the Agreement States on an annual basis and maintain records of such reports, as well as meet existing information collection requirements in 10 CFR Parts 19 and 20. In addition, labeling requirements and notifications to recipients would be required for certain initial distributions of source material. Proposed revisions to the general license provisions in § 40.22 would specifically require the general licensee to respond to NRC requests for information in a timely manner and notify the NRC when ceasing activities if significant contamination is identified. NOTE: This proposed rule affects information collections in Parts 19, 20, and 40 as well as NRC Form 313/313A series of forms. Information collections for Parts 19 and 40 have both been entered in ROCIS under Part 40 because Part 19 will soon be undergoing OMB review for renewal (expiration date of 11/30/10). Information collections for Part 20 and NRC Form 313 have been entered into ROCIS under their appropriate clearance numbers.

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Authorizing Statute(s): PL: Pub.L. 83 - 703 1-311 Name of Law: Atomic Energy Act
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
3150-AH15	Proposed rulemaking	75 FR 43425	07/26/2010

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Federal Register Notices & Comments

Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 1

IC Title	Form No.	Form Name
NRC Form 313, Application for Material License, NRC Form 313A, Medical use Training and Experience and Preceptor Attestation.	NRC313A(AUD), NRC313A(AMP), NRC-313, NRC-313A, NRC313A(ANP), NRC313A(AUS), NRC313A(AUT)	Application for Material License ,   NRC Form 313A Series (RSO) ,   NRC Form 313A (AMP) ,   NRC Form 313A (AUD) ,   NRC Form 313A(ANP) ,   NRC Form 313A(AUS) ,   NRC Form 313A(AUT)

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Burden increases because of Program Change due to Agency Discretion: Yes

Burden Increase Due to: Changing Regulations

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement: The proposed rule would add a requirement in 10 CFR 40.13(c)(10) that requires persons who initially transfer products for use under a product exemption in 10 CFR 40.13(c) to obtain a specific license to be issued under the proposed 10 CFR 40.52 requirements. This means that those persons who previously operated as general licensees (and therefore did not have to submit an application to the NRC) and manufacture and initially distribute products for use under 10 CFR 40.13(c) must now be licensed as specific licensees. To become specific licensees, they must submit an application (NRC Form 313, “Application for Materials License”) to the NRC. An estimated 11 licensees would be required to submit NRC Form 313 as an application to become specific licensees. NOTE: Federal government costs for this proposed rule associated with NRC Form 313 are estimated at $22,128. Total government costs associated with this proposed rule are $24,120.

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Annual Cost to Federal Government: $2,442,469

Does this IC contain surveys, censuses, or employ statistical methods? No

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? No

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).

The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(i) Why the information is being collected;

(ii) Use of information;

(iii) Burden estimate;

(iv) Nature of response (voluntary, required for a benefit, or mandatory);

(v) Nature and extent of confidentiality; and

(vi) Need to display currently valid OMB control number;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.

Certification Date: 08/12/2010

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