Medical Use of Byproduct Material -- 10 CFR 35

Forms and Documents

Document Name	Status

No forms / supporting documents in this ICR. Check IC Document Collections.

IC Document Collections

IC ID	Document Title	Status
33146	Medical Use of Byproduct Material -- 10 CFR 35	Migrated

ICR Details

OMB Control No: 3150-0010	ICR Reference No: 199607-3150-001
Status: Historical Active	Previous ICR Reference No: 199503-3150-013
Agency/Subagency: NRC	Agency Tracking No:
Title: Medical Use of Byproduct Material -- 10 CFR 35
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 09/19/1996
	Date Received in OIRA: 07/16/1996
Terms of Clearance: This collection of information is approved through September 30, 1999. However, it is unclear that the collection represents the least burdensome approach to achieve the safety goals of the commission. We understand that the 10 CFR 35 program is being reviewed by the Agency, and assume that the burden associated with compliance with the current program will be reduced as a result of this review. Future submissions should include a discussion of NRC's progress in achieving these reductions.

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	09/30/1999	09/30/1999	09/30/1996
Responses	6,587,935	0	3,220,723
Time Burden (Hours)	1,319,277	0	329,793
Cost Burden (Dollars)	0	0	0

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Abstract: 10 CFR 35 contains requirements that apply to NRC licensees who are authorized to administer byproduct material or its radiation to humans for medical use. The information is required to ensure that public health and safety are protected and that the licensee possession and use of byproduct material is in compliance with license and regulatory requirements.

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Authorizing Statute(s): None

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:

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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
Medical Use of Byproduct Material -- 10 CFR 35

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ICR Summary of Burden

	Total Approved	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	6,587,935	3,220,723	0	0	3,367,212	0
Annual Time Burden (Hours)	1,319,277	329,793	0	0	989,484	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

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

Burden Increase Due to:

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

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $0

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]? Uncollected

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? Uncollected

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? Uncollected

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: 07/16/1996

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