0910-AG04 200710 The Regulatory Plan and the Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Amendment to the Current Good Manufacturing Practice Regulations for Finished Pharmaceuticals Routine and Frequent First Time Published in The Unified Agenda Proposed Rule Stage No No 21 CFR 210 to 211 21 USC 321 21 USC 351 to 352 21 USC 355 21 USC 360b 21 USC 371 21 USC 374 42 USC 216 42 USC 262 42 USC 263a to 264 No NPRM-Companion to Direct Final Rule 11/00/2007 Direct Final Rule 11/00/2007 No None No No Not Collected Jessica Tave 0910 Food and Drug Administration FDA 301 827-6190 Center for Biologics Evaluation and Research, 1401 Rockville Pike, Suite 200N, HFM-600, Rockville MD 20852