Federal (United States) · Session law
Pub. L. 102-571 — To amend the Federal Food, Drug, and Cosmetic Act to authorize human drug application, prescription drug establishment, and prescription drug product fees and for other purposes.
14 sections
14 sections
- Pub. L. 102-571, tit. I, sec. 101SHORT TITLE AND REFERENCE.Enacted
- Pub. L. 102-571, tit. I, sec. 102FINDINGS.Enacted
- Pub. L. 102-571, tit. I, sec. 103FEES RELATING TO DRUGS.Enacted
- Pub. L. 102-571, tit. I, sec. 104ANNUAL REPORTS.Enacted
- Pub. L. 102-571, tit. I, sec. 105SUNSET.Enacted
- Pub. L. 102-571, tit. I, sec. 106CONFORMING AMENDMENTS TO CHAPTER VIIEnacted
- Pub. L. 102-571, tit. I, sec. 107GENERAL CONFORMING AMENDMENTS.Enacted
- Pub. L. 102-571, tit. I, sec. 108ANIMAL DRUG USER FEE STUDY.Enacted
- Pub. L. 102-571, tit. II, sec. 201SHORT TITLE.Enacted
- Pub. L. 102-571, tit. II, sec. 202PROHIBITION.Enacted
- Pub. L. 102-571, tit. II, sec. 203UNITED STATES RECOMMENDED DAILY ALLOWANCES.Enacted
- Pub. L. 102-571, tit. II, sec. 204ENFORCEMENT REPORT.Enacted
- Pub. L. 102-571, tit. II, sec. 205MANAGEMENT ACTIVITIES STUDY.Enacted
- Pub. L. 102-571, tit. II, sec. 206SAFETY AND REGULATORY OUTCOMES STUDY.Enacted