The Federal Food, Drug, and Cosmetic Act and subsequent amending statutes are codified into Title 21 Chapter 9 of the United States Code.

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 …

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 …

To search the FD&C Act on the Law Revision Counsel website, you may either search by U.S. code section number or browse the Title 21 section listing. Sec. 356. Expedited approval of …

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 …

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 …

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 …

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.

21 u.s. code chapter 9 - federal food, drug, and cosmetic act . u.s. code ; prev | next. subchapter i—short title (section 301) subchapter ii—definitions (§§ 321 – 321d) subchapter iii—prohibited …

在1983年，由Henry Waxman（是不是很眼熟）发起的孤儿药法案（Orphan Drug Act of 1983）立法通过。 根据法案内容，如果药物、疫苗和诊断试剂旨在治疗患病不足 200,000 名美国公民 …