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- [21] The Food and Drug Administration's (FDA's) 510(k) Process: A Systematic Review of 1000 Cases AMERICAN JOURNAL OF MEDICINE, 2023, 136 (02): : 172 - 178.e14
- [23] US Food and Drug Administration Regulations and Birth Defect Prevention: It's More Than Labeling BIRTH DEFECTS RESEARCH, 2018, 110 (09): : 737 - 737
- [24] Information to Improve Public Perceptions of the Food and Drug Administration (FDA's) Tobacco Regulatory Role INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, 2018, 15 (04):
- [26] Food and Dietary Supplement Package Labeling-Guidance from FDA's Warning Letters and Title 21 of the Code of Federal Regulations COMPREHENSIVE REVIEWS IN FOOD SCIENCE AND FOOD SAFETY, 2016, 15 (01): : 92 - 129
- [27] Do drug package inserts meet the rules and regulations of Iran's Food and Drug Administration in terms of informing patients? HEALTH PROMOTION PERSPECTIVES, 2019, 9 (03): : 214 - 222
- [28] Evaluation of Pediatric Dosing Recommendations in the Food and Drug Administration (FDA) Approved Labeling of Anti-Infective Products. PHARMACOTHERAPY, 2018, 38 (04): : E37 - E37