0910-AB93 200104 Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Periodic Testing for Certain Human Drug, Veterinary Drug, and Biological Product Final Specifications The proposed rule requests comments on when certain finished product laboratory tests to determine satisfactory conformance to final specifications for new human drug, animal drug, animal drugs and biological products may be performed on a periodic basis. Other Significant Previously Published in The Unified Agenda Proposed Rule Stage Undetermined Undetermined 21 CFR 211.165 21 CFR 314 21 CFR 514 21 CFR 601 21 CFR 610 21 USC 321 21 USC 351 21 USC 352 21 USC 355 21 USC 360(b) 21 USC 371 21 USC 374 No NPRM 11/00/2001 Undetermined No Undetermined NA Not Collected Carol Drew 0910 Food and Drug Administration FDA 301 796-3601 301 847-8440 Suite 3037 (HFD-7), Center for Drug Evaluation and Research, WO 51, Room 6306, 10903 New Hampshire Avenue, Silver Spring MD 20993-0002 Not Procurement Related No