0910-AA57 199510 The Regulatory Plan and the Unified Agenda of Federal Regulations 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Streamlining Procedures for Changes in Production of Biologics Other Significant First Time Published in The Unified Agenda Proposed Rule Stage 21 CFR 601 15 USC 1451 to 1461 21 USC 321 21 USC 351 to 353 21 USC 355 21 USC 360 21 USC 360c to 360f 21 USC 360u to 360j 21 USC 371 21 USC 374 21 USC 379e 21 USC 381 42 USC 216 42 USC 241 42 USC 262 to 263 Yes NPRM 01/00/1996 Yes Businesses None NA Not Collected Tracey Forfa 0910 Food and Drug Administration FDA 301 594-3074 Suite 200N (HFM-630), Center for Biologics Evaluation and Research, 1401 Rockville Pike, Rockville MD 20852-1448 Revising Text to Reduce Burden or Duplication, or Streamline Requirements