[Federal Register Volume 74, Number 73 (Friday, April 17, 2009)]
[Notices]
[Page 17871]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: E9-8776]


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DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. FDA-2008-N-0345]


Agency Information Collection Activities; Announcement of Office 
of Management and Budget Approval; Current Good Manufacturing Practices 
and Related Regulations for Blood and Blood Components; and 
Requirements for Donor Testing, Donor Notification, and ``Lookback''

AGENCY:  Food and Drug Administration, HHS.

ACTION:  Notice.

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SUMMARY:  The Food and Drug Administration (FDA) is announcing that a 
collection of information entitled ``Current Good Manufacturing 
Practices and Related Regulations for Blood and Blood Components; and 
Requirements for Donor Testing, Donor Notification, and `Lookback''' 
has been approved by the Office of Management and Budget (OMB) under 
the Paperwork Reduction Act of 1995.

FOR FURTHER INFORMATION CONTACT: Jonna Capezzuto, Office of Information 
Management (HFA-710), Food and Drug Administration, 5600 Fishers Lane, 
Rockville, MD 20857, 301-796-3794.

SUPPLEMENTARY INFORMATION: In the Federal Register of November 12, 2008 
(73 FR 66901), the agency announced that the proposed information 
collection had been submitted to OMB for review and clearance under 44 
U.S.C. 3507. An agency may not conduct or sponsor, and a person is not 
required to respond to, a collection of information unless it displays 
a currently valid OMB control number. OMB has now approved the 
information collection and has assigned OMB control number 0910-0116. 
The approval expires on February 29, 2012. A copy of the supporting 
statement for this information collection is available on the Internet 
at http://www.reginfo.gov/public/do/PRAMain.

    Dated: April 10, 2009.
Jeffrey Shuren,
Associate Commissioner for Policy and Planning.
[FR Doc. E9-8776 Filed 4-16-09; 8:45 am]
BILLING CODE 4160-01-S