10 CFR 30, Rules of General Applicability to Domestic Licensing of Byproduct Material

Forms and Documents

Document Name	Status
Revised Guidance for the ICBMIP Proposed Rule DCC.docx Supplementary Document	2022-06-23
Regulatory Analysis for 30-32 proposed rule.pdf Supplementary Document	2022-06-23
ICBMIP Part 30 OMB supporting statement as of 6-23.docx Supporting Statement A	2022-06-23

IC Document Collections

IC ID	Document Title	Status
33212	10 CFR 30, Rules of General Applicability to Domestic Licensing of Byproduct Material	Modified

ICR Details

OMB Control No: 3150-0017	ICR Reference No: 202206-3150-002
Status: Received in OIRA	Previous ICR Reference No: 201909-3150-003
Agency/Subagency: NRC	Agency Tracking No:
Title: 10 CFR 30, Rules of General Applicability to Domestic Licensing of Byproduct Material
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular	Date Submitted to OIRA: 06/27/2022

	Requested	Previously Approved
Expiration Date	01/31/2023	01/31/2023
Responses	155,182	155,164
Time Burden (Hours)	228,864	228,279
Cost Burden (Dollars)	11,931	11,926

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Abstract: PROPOSED RULE - 10 CFR Parts 30 and 32, Items Containing Byproduct Material Incidental to Production. 10 CFR part 30 establishes requirements that are applicable to all persons in the United States governing domestic licensing of radioactive byproduct material. The application, reporting and recordkeeping requirements are necessary to permit the NRC to make a determination whether the possession, use, and transfer of byproduct material is in conformance with the Commission's regulations for protection of the public health and safety. This proposed rule would amend 10 CFR part 30 to add a new class exemption from licensing requirements for items containing byproduct material incidental to their production and amend 10 CFR part 32 to add new sections for distribution requirements.

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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-AJ54	Proposed rulemaking	87 FR 38012	06/27/2022

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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
10 CFR 30, Rules of General Applicability to Domestic Licensing of Byproduct Material

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ICR Summary of Burden

	Total Request	Previously Approved	Change Due to New Statute	Change Due to Agency Discretion	Change Due to Adjustment in Estimate	Change Due to Potential Violation of the PRA
Annual Number of Responses	155,182	155,164	0	18	0	0
Annual Time Burden (Hours)	228,864	228,279	0	585	0	0
Annual Cost Burden (Dollars)	11,931	11,926	0	5	0	0

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 burden would increase by 585 hours (540 reporting + 45 recordkeeping) from 228,279 hours to 228,864 hours as a result of the proposed rule.

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Annual Cost to Federal Government: $1,561,450

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

Does this ICR request any personally identifiable information (see OMB Circular No. A-130 for an explanation of this term)? Please consult with your agency's privacy program when making this determination.     No

Does this ICR include a form that requires a Privacy Act Statement (see 5 U.S.C. §552a(e)(3))? Please consult with your agency's privacy program when making this determination.     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? No

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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: 06/27/2022

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