View Information Collection Request (ICR) Package

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View ICR - OIRA Conclusion

OMB Control No: 3150-0010	ICR Reference No: 200708-3150-003
Status: Historical Active	Previous ICR Reference No: 200410-3150-001
Agency/Subagency: NRC	Agency Tracking No:
Title: 10 CFR 35, Medical Use of Byproduct Material
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: 12/04/2007
	Date Received in OIRA: 08/15/2007
Terms of Clearance:

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	12/31/2010	36 Months From Approved	12/31/2007
Responses	259,332	0	244,086
Time Burden (Hours)	987,764	0	1,113,217
Cost Burden (Dollars)	79,079	0	67,000

ICR Summary of Burden

	Total Approved	Previously Approved	Change Due to Agency Discretion
Annual Number of Responses	259,332	244,086	15,246
Annual Time Burden (Hours)	987,764	1,113,217	-125,453
Annual Cost Burden (Dollars)	79,079	67,000	12,079

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: Yes

Burden Reduction Due to: Changing Regulations

Short Statement: The burden reduction is attributable to two causes: (1)the loss of a one-time burden associated with the submission of preceptor statements in accordance with the amended 35.14(a); and (2) one-time activities that specialty boards are required to undertake, in order to become recognized by the NRC as entities capable of certifying licensees' training to effectively carry out duties under Part 35. In addition, Subpart J contained training and experience requirements and associated reporting requirements that were effective during the last reporting period. However, the Subpart J training and experience and any associated reporting expired as of October 24, 2005.

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