0910-AA49 200310 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 Foreign and Domestic Establishment Registration and Listing Requirements for Drugs and Biologics Other Significant Previously Published in The Unified Agenda Proposed Rule Stage No No 21 CFR 20 21 CFR 201 21 CFR 207 21 CFR 314 21 CFR 330 21 CFR 514 21 CFR 515 21 CFR 601 21 CFR 607 21 CFR 610 21 CFR 1271 21 USC 321 21 USC 331 21 USC 351 21 USC 352 21 USC 355 21 USC 360 21 USC 360b 21 USC 371 21 USC 374 42 USC 262 42 USC 264 42 USC 271 No NPRM 03/00/2004 Yes Businesses None No NA Not Collected Mary Keyes H. 0910 Food and Drug Administration FDA 301 594-2041 301 827-5562 Suite 3037 (HFD-7), Center for Drug Evaluation and Reserach, 1451 Rockville Pike, Rockville MD 20852