[Federal Register Volume 66, Number 198 (Friday, October 12, 2001)]
[Notices]
[Page 52140]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 01-25659]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Food and Drug Administration

[Docket No. 01N-0176]


Agency Information Collection Activities; Announcement of OMB 
Approval; Good Laboratory Practices (GLP) Regulations for Nonclinical 
Laboratory Studies

AGENCY: Food and Drug Administration, HHS.

ACTION: Notice.

-----------------------------------------------------------------------

SUMMARY: The Food and Drug Administration (FDA) is announcing that a 
collection of information entitled ``Good Laboratory Practices (GLP) 
Regulations for Nonclinical Laboratory Studies'' has been approved by 
the Office of Management and Budget (OMB) under the Paperwork Reduction 
Act of 1995.

FOR FURTHER INFORMATION CONTACT: JonnaLynn P. Capezzuto, Office of 
Information Resources Management (HFA-250), Food and Drug 
Administration, 5600 Fishers Lane, Rockville, MD 20857, 301-827-4659.

SUPPLEMENTARY INFORMATION: In the Federal Register of July 20, 2001 (66 
FR 37977), 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 0910-0119. 
The approval expires on September 30, 2004. A copy of the supporting 
statement for this information collection is available on the Internet 
at http://www.fda.gov/ohrms/dockets.

    Dated: October 5, 2001.
Margaret M. Dotzel,
Associate Commissioner for Policy.
[FR Doc. 01-25659 Filed 10-11-01; 8:45 am]
BILLING CODE 4160-01-S