02-26875. Agency Information Collection Activities; Announcement of OMB Approval; Postmarketing Adverse Drug Experience Reporting
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Start Preamble
AGENCY:
Food and Drug Administration, HHS.
ACTION:
Notice.
SUMMARY:
The Food and Drug Administration (FDA) is announcing that a collection of information entitled “Postmarketing Adverse Drug Experience Reporting” has been approved by the Office of Management and Budget (OMB) under the Paperwork Reduction Act of 1995 (the PRA).
Start Further InfoFOR FURTHER INFORMATION CONTACT:
Karen L. Nelson, Office of Information Resources Management (HFA-250), Food and Drug Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-827-1482.
End Further Info End Preamble Start Supplemental InformationSUPPLEMENTARY INFORMATION:
In the Federal Register of July 22, 2002 (67 FR 47821), 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 0910-0230. The approval expires on September 30, 2005. A copy of the supporting statement for this information collection is available on the Internet at http://www.fda.gov/ohrms/dockets.
Start SignatureDated: October 16, 2002.
Margaret M. Dotzel,
Associate Commissioner for Policy.
[FR Doc. 02-26875 Filed 10-22-02; 8:45 am]
BILLING CODE 4160-01-S
Document Information
- Published:
- 10/23/2002
- Department:
- Food and Drug Administration
- Entry Type:
- Notice
- Action:
- Notice.
- Document Number:
- 02-26875
- Pages:
- 65130-65130 (1 pages)
- Docket Numbers:
- Docket No. 02N-0012
- PDF File:
- 02-26875.pdf