[Federal Register Volume 63, Number 221 (Tuesday, November 17, 1998)] [Notices] [Pages 63935-63936] From the Federal Register Online via the Government Publishing Office [www.gpo.gov] [FR Doc No: 98-30609] ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. 98N-0335] 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 (the PRA).
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 September 25, 1998 (63 FR 51357), the agency announced that the proposed information collection had been submitted to OMB for review and clearance under section 3507 of the PRA (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 October 31, 2001.
Dated: November 4, 1998. William K. Hubbard, Associate Commissioner for Policy Coordination. [FR Doc. 98-30609 Filed 11-16-98; 8:45 am] BILLING CODE 4160-01-F