Federal (United States) · Session law
Title IX
20 sections
20 sections
- Pub. L. 110-85, tit. IX, subtit. A, sec. 901POSTMARKET STUDIES AND CLINICAL TRIALS REGARDING HUMAN DRUGS; RISK EVALUATION AND MITIGATION STRATEGIES.Enacted
- Pub. L. 110-85, tit. IX, subtit. A, sec. 902ENFORCEMENT.Enacted
- Pub. L. 110-85, tit. IX, subtit. A, sec. 903NO EFFECT ON WITHDRAWAL OR SUSPENSION OF APPROVAL.Enacted
- Pub. L. 110-85, tit. IX, subtit. A, sec. 904BENEFIT-RISK ASSESSMENTS.Enacted
- Pub. L. 110-85, tit. IX, subtit. A, sec. 905ACTIVE POSTMARKET RISK IDENTIFICATION AND ANALYSIS.Enacted
- Pub. L. 110-85, tit. IX, subtit. A, sec. 906STATEMENT FOR INCLUSION IN DIRECT-TO-CONSUMER ADVERTISEMENTS OF DRUGS.Enacted
- Pub. L. 110-85, tit. IX, subtit. A, sec. 907NO EFFECT ON VETERINARY MEDICINE.Enacted
- Pub. L. 110-85, tit. IX, subtit. A, sec. 908AUTHORIZATION OF APPROPRIATIONS.Enacted
- Pub. L. 110-85, tit. IX, subtit. A, sec. 909EFFECTIVE DATE AND APPLICABILITY.Enacted
- Pub. L. 110-85, tit. IX, subtit. B, sec. 911CLINICAL TRIAL GUIDANCE FOR ANTIBIOTIC DRUGS.Enacted
- Pub. L. 110-85, tit. IX, subtit. B, sec. 912PROHIBITION AGAINST FOOD TO WHICH DRUGS OR BIOLOGICAL PRODUCTS HAVE BEEN ADDED.Enacted
- Pub. L. 110-85, tit. IX, subtit. B, sec. 913ASSURING PHARMACEUTICAL SAFETY.Enacted
- Pub. L. 110-85, tit. IX, subtit. B, sec. 914CITIZEN PETITIONS AND PETITIONS FOR STAY OF AGENCY ACTION.Enacted
- Pub. L. 110-85, tit. IX, subtit. B, sec. 915POSTMARKET DRUG SAFETY INFORMATION FOR PATIENTS AND PROVIDERS.Enacted
- Pub. L. 110-85, tit. IX, subtit. B, sec. 916ACTION PACKAGE FOR APPROVAL.Enacted
- Pub. L. 110-85, tit. IX, subtit. B, sec. 917RISK COMMUNICATION.Enacted
- Pub. L. 110-85, tit. IX, subtit. B, sec. 918REFERRAL TO ADVISORY COMMITTEE.Enacted
- Pub. L. 110-85, tit. IX, subtit. B, sec. 919RESPONSE TO THE INSTITUTE OF MEDICINE.Enacted
- Pub. L. 110-85, tit. IX, subtit. B, sec. 920DATABASE FOR AUTHORIZED GENERIC DRUGS.Enacted
- Pub. L. 110-85, tit. IX, subtit. B, sec. 921ADVERSE DRUG REACTION REPORTS AND POSTMARKET SAFETY.Enacted