10 CFR Part 32, Specific Domestic Licenses to Manufacture or Transfer Certain Items Containing Byproduct Material

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
10CFR32FinalSSamended[6].doc	Supporting Statement A	Uploaded 2009-06-02	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
33107	10 CFR Part 32, Specific Domestic Licenses to Manufacture or Transfer Certain Items Containing Byproduct Material		Modified
184661	10 CFR Part 32, Specific Domestic Licenses to Manufacture or Transfer Certain Items Containing Byproduct Material		Removed

ICR Details

OMB Control No: 3150-0001	ICR Reference No: 200811-3150-002
Status: Historical Inactive	Previous ICR Reference No: 200804-3150-007
Agency/Subagency: NRC	Agency Tracking No:
Title: 10 CFR Part 32, Specific Domestic Licenses to Manufacture or Transfer Certain Items Containing Byproduct Material
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Withdrawn and continue	Conclusion Date: 06/08/2009
	Date Received in OIRA: 11/18/2008
Terms of Clearance: Supporting Statement amended per agency request and also to reflect indadvertently blank items on certification (see Item 18). Withdrawn due to procedural errors. To be resubmitted with corrections.

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	11/30/2008	36 Months From Approved	07/31/2009
Responses	3,402	0	3,402
Time Burden (Hours)	179,188	0	179,188
Cost Burden (Dollars)	7,000	0	7,000

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Abstract: 10 CFR 32 establishes requirements for specific licenses for the introduction of byproduct material into products or materials and transfer of the products or materials to general licensees or persons exempt from licensing, medical use product distributors to specific licensees, and those requesting a certificate of registration for a sealed source and/or device. It also prescribes requirements governing holders of the specific licenses. Some of the requirements are for information which must be submitted in an applicaiton for a certificate of registration for a sealed source and/or device, records which must be kept, reports which must be submitted, and information which must be forwarded to general licensees and persons exempt from licensing. As mentioned, 10 CFR 32 also prescribes requirements for the issuance of certiificates of registration (concerning radiation safety information about a product) to manufacturers or initial tranferors of sealed sources and devices. Submission or retention of the information is mandatory for persons subject to the 10 CFR 32 requirements. The information is used by the NRC to make licensing and other regulatory determinations concerning the use of radioactive byproduct material in products and devices.

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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:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	73 FR 20071	04/14/2008
30-day Notice:	Federal Register Citation:	Citation Date:
	73 FR 42374	07/21/2008
Did the Agency receive public comments on this ICR? No

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

table that charts list of burden

IC Title	Form No.	Form Name
10 CFR Part 32, Specific Domestic Licenses to Manufacture or Transfer Certain Items Containing Byproduct Material
10 CFR Part 32, Specific Domestic Licenses to Manufacture or Transfer Certain Items Containing Byproduct Material

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

Burden Increase Due to: Miscellaneous Actions

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

Burden Reduction Due to: Miscellaneous Actions

Short Statement: Though some increases in burden hours were noted, overall a decrease in estimated burden hours outweighed the increases as illustrated below: a. The burden estimate has been corrected downward by eliminating double counting of respondents under certain similar categories. b. Exempt distribution license review has been eliminated since the application review costs are already reported under OMB Clearance No. 3150-0120 for NRC Form 313. c. The total number of recordkeepers has decreased from 975 to 616 to more accurately reflect current data in the License Tracking System and Agreement State data which resulted in a decrease of total burden hours. d. There is a reduction in the number of respondents for Section 32.210 by 164 respondents from 600 to 224; the number of responses by 752 from 1,200 to 448 responses; and the burden by 15,792 hours from 25,200 to 9,408 hours. This reduction is based on the current number of actions worked on rather than the total number of registrants, thereby making the overall burden reduction for this section, an estimated 12,684 hours, an agency adjustment. The overall burden for this clearance has decreased by an estimated 12,684 hours from the currently approved burden of 179,188 hours to the proposed burden of 166,504 hours. The ROCIS Edit IC Worksheet for 3150-0001 (10 CFR Part 32), currently submitted to OMB for approval, shows a “Program Change Due to Agency Discretion” of 42,997 hours because of an error which occurred when data was entered into OMB’s ROCIS electronic data system for an 83-C correction worksheet for this package which was submitted to OMB for review on 5/14/2008, and which was approved by OMB on 11/9/2008. When the current (2009) Part 32 ROCIS package was opened for processing, it contained two separate ICs split into beginning balances of 136,191 and 42,997 hours. To clarify this within the package, upon the advice of an OMB contractor, the 42,997 hour IC was removed, and its balance was added to the remaining IC within the package as a “Program Change Due to Agency Discretion.”

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Annual Cost to Federal Government: $2,195,488

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)? 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: 11/18/2008

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