Displaying title 21, up to date as of 3/20/2025. Title 21 was last amended 2/25/2025. Choosing an item from citations and headings will bring you directly to the content. Choosing an item from …

(a) It is impracticable to list all substances that are generally recognized as safe for their intended use. However, by way of illustration, the Commissioner regards such common food ingredients …

(a) The regulations in this part contain the minimum current good manufacturing practice for preparation of drug products (excluding positron emission tomography drugs) for …

【US—FDA 21CFR】指的是《美国联邦法规》 (CFR) 第21条， 有关食品、药品、医疗器械、辐射类电子产品、化妆品、烟草制品d等产品在FDA监管下达到其相应标准。 1. FDA是指 美国 …

Title 21 of the CFR is reserved for rules of the Food and Drug Administration. Each title (or volume) of the CFR is revised once each calendar year. A revised Title 21 is issued on...

Title 21 is the portion of the Code of Federal Regulations that governs food and drugs within the United States for the Food and Drug Administration (FDA), the Drug Enforcement …

2015年5月19日 · 从21 CFR Part11的目录看整个法规分为3章，分别是： A章节—一般规定 11.1适用范围 （21 CFR Part 11的适用范围，什么情况下的电子记录和电子签名是适用于21CFR …

cfr ; prev | next. chapter i—food and drug administration, department of health and human services (subchapters a - l) chapter ii—drug enforcement administration, department of justice …

凡是在药品生产、加工、包装或储存过程中存在任何不符合本部分及 21cfr 211，225， 226 部分的法规，则依据 ffdca 501(a)(2)(b)，该药品应视为伪劣药；并对该事故的责任 人采取相应监管 …

2024年12月24日 · For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR). Note: If you need help accessing information in different file …