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HHS/FDA

RIN: 0910-AA69

Publication ID: Spring 1996

Title: ●Reinvention of Regulations
Abstract: FDA is considering ways to further streamline certain regulations that are outdated or otherwise in need of reform. The agency is taking this action in response to President Clinton's March 4, 1995 directive to all Federal agencies to conduct a page-by-page review of their regulations as part of the "Reinventing Government" initiative. FDA plans to reinvent approximately 45 percent of its regulations to ease the burden on regulated industry and consumers without sacrificing public health protection. For those regulations requiring Congressional permission to reinvent, the Administration will seek legislative changes.
Agency: Department of Health and Human Services(HHS)	Priority: Other Significant
RIN Status: First time published in the Unified Agenda	Agenda Stage of Rulemaking: Prerule Stage
CFR Citation: 21 CFR 1 to 3 21 CFR 5 21 CFR 10 21 CFR 12 21 CFR 19 to 20 21 CFR 56 21 CFR 58 21 CFR 70 to 71 21 CFR 80 21 CFR 101 21 CFR 170 21 CFR 172 to 175 21 CFR 177 to 178 21 CFR 184 21 CFR 730 to 740 ... (To search for a specific CFR, visit the Code of Federal Regulations.)
Legal Authority: 5 USC 504 5 USC 551 to 558 5 USC 701 to 721 7 USC 138 7 USC 2271 15 USC 402 15 USC 409 15 USC 638 15 USC 1261 to 1282 15 USC 1451 to 1461 15 USC 3701 to 3711 21 USC 41 to 50 21 USC 61 to 63 21 USC 141 to 149 21 USC 321 to 394

Timetable:

Action	Date	FR Cite
ANPRM	06/00/1996

Regulatory Flexibility Analysis Required: Yes	Government Levels Affected: Federal, Local, State, Tribal
Small Entities Affected: Businesses, Governmental Jurisdictions, Organizations
Included in the Regulatory Plan: No
Agency Contact: Lisa M. Helmanis Office of Policy (HF-26) Department of Health and Human Services Food and Drug Administration 5600 Fishers Lane, Rockville, MD 20857 Phone:301 443-3480