0910-AC25 200204 Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Exception From General Requirements for Informed Consent; Request for Comments and Information Other Significant Previously Published in The Unified Agenda Proposed Rule Stage No No 21 CFR 50.23 21 USC 321 21 USC 346 21 USC 346a 21 USC 348 21 USC 352 21 USC 353 21 USC 355 21 USC 360 21 USC 360bbb 21 USC 360c 21 USC 360d 21 USC 360e 21 USC 360f 21 USC 360h 21 USC 360i 21 USC 360j 21 USC 371 21 USC 379e 21 USC 381 42 USC 241 42 USC 262 42 USC 263b-263n Yes NPRM 06/00/2002 No No None No NA Not Collected Bonnie Lee M. 0910 Food and Drug Administration FDA 301 827-1259 301 827-1169 blee@oc.fda.gov Room 9C24 (HF-34), Office of Good Clinical Practice, Office of Science Coordination & Communication, 5600 Fishers Lane, Rockville MD 20857 Not Procurement Related