Federal (United States) · Session law
Subtitle E
10 sections
10 sections
- Pub. L. 117-328, div. FF, tit. II, subtit. E, ch. 1, sec. 2501ACCELERATING COUNTERMEASURE DEVELOPMENT AND REVIEW.Enacted
- Pub. L. 117-328, div. FF, tit. II, subtit. E, ch. 1, sec. 2502THIRD PARTY TEST EVALUATION DURING EMERGENCIES.Enacted
- Pub. L. 117-328, div. FF, tit. II, subtit. E, ch. 1, sec. 2503PLATFORM TECHNOLOGIES.Enacted
- Pub. L. 117-328, div. FF, tit. II, subtit. E, ch. 1, sec. 2504INCREASING EUA DECISION TRANSPARENCY.Enacted
- Pub. L. 117-328, div. FF, tit. II, subtit. E, ch. 1, sec. 2505IMPROVING FDA GUIDANCE AND COMMUNICATION.Enacted
- Pub. L. 117-328, div. FF, tit. II, subtit. E, ch. 2, sec. 2511ENSURING REGISTRATION OF FOREIGN DRUG AND DEVICE MANUFACTURERS.Enacted
- Pub. L. 117-328, div. FF, tit. II, subtit. E, ch. 2, sec. 2512EXTENDING EXPIRATION DATES FOR CERTAIN DRUGS.Enacted
- Pub. L. 117-328, div. FF, tit. II, subtit. E, ch. 2, sec. 2513COMBATING COUNTERFEIT DEVICES.Enacted
- Pub. L. 117-328, div. FF, tit. II, subtit. E, ch. 2, sec. 2514PREVENTING MEDICAL DEVICE SHORTAGES.Enacted
- Pub. L. 117-328, div. FF, tit. II, subtit. E, ch. 2, sec. 2515TECHNICAL CORRECTIONS.Enacted