Federal Food, Drug, and Cosmetic Act (FD&C Act) | FDA
The Federal Food, Drug, and Cosmetic Act and subsequent amending statutes are codified into Title 21 Chapter 9 of the United States Code.
Federal Food, Drug, and Cosmetic Act of 1938 - Wikipedia
The United States Federal Food, Drug, and Cosmetic Act (abbreviated as FFDCA, FDCA, or FD&C) is a set of laws passed by the United States Congress in 1938 giving authority to the U.S. Food and Drug Administration (FDA) to oversee the …
Laws, Acts, and Rules | FDA
2023年8月21日 · Visit the FDA Regulatory Information Web page for information on the Federal Food, Drug, and Cosmetic Act (FD&C Act), Food and Drug Administration Amendments Act (FDAAA) of 2007, and...
Laws Enforced by FDA | FDA - U.S. Food and Drug Administration
The FD&C Act completely overhauled the public health system. Among other provisions, the law authorized the FDA to demand evidence of safety for new drugs, issue standards for food, and conduct...
联邦食品、药品和化妆品法案 - 维基百科，自由的百科全书
美国 联邦食品、药品和化妆品法案 （常缩写为 FFDCA， FDCA，或 FD&C）是 美国国会 在1938年通过的一系列法案的总称，赋予 美国食品药品监督管理局 （FDA）监督监管食品安全、药品、及化妆品的权力。 该法案主要是由 Royal S. Copeland 写成，其为一三年期的纽约州参议员。 [2] 该法案通过后又历经多次修改。 催生该法案的主要原因之一是因为一种 磺胺 药物中所使用的溶剂 二甘醇 导致100多名病人死亡。 [3] 这部法案诞生后取代了1906年通过的 纯净食品及药品 …
Food, Drug, and Cosmetic Act - StatPearls - NCBI Bookshelf
2023年7月31日 · The 1938 Federal Food, Drug, and Cosmetic Act (FDCA) is a set of United States (US) laws that authorize the Food and Drug Administration (FDA) to oversee and regulate the production, sale, and distribution of food, drugs, medical devices, and cosmetics.
To amend the Federal Food, Drug, and Cosmetic Act and the Public Health Service Act to improve the regulation of food, drugs, devices, and biological products, and for other purposes.
FDA药品监管法律法规整理合集 - 知乎 - 知乎专栏
《食品、药品和化妆品法案》 （<The Food, Drug and Cosmetic Act>，FD&C Act） 早期的美国医药市场混乱不堪，因为当时科技水平的局限性，导致各种“万能神药”充斥市场，尽管美国早在1906年就颁布了《食品、药品纯净法案》（<Pure Food and Drug Act>），在1930年就正式成立 ...
Food and Drug Administration Amendments Act of 2007
To amend the Federal Food, Drug, and Cosmetic Act to revise and extend the user-fee programs for prescription drugs and for medical devices, to enhance the postmarket authorities of the Food and Drug Administration with respect to the safety of drugs, and for other purposes.
Food and Drug Administration Modernization Act of 1997
The United States Food and Drug Administration Modernization Acts (FDAMA) are amendments to the Federal Food, Drug, and Cosmetic Act, which regulated products by the FDA. The first bill, the FDA Modernization Act of 1997, reduced the timeline for approving new pharmaceutical drugs. It also loosened rules around broadcast pharmaceutical advertising.