
eCFR :: Title 21 of the CFR -- Food and Drugs
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 full text search results will bring you to those results. Pressing enter in the search box will also bring you to search results.
21 CFR Part 182 -- Substances Generally Recognized as Safe
(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 as salt, pepper, vinegar, baking powder, and monosodium glutamate as safe for their intended use.
eCFR :: 21 CFR Part 211 -- Current Good Manufacturing …
(a) The regulations in this part contain the minimum current good manufacturing practice for preparation of drug products (excluding positron emission tomography drugs) for administration to humans or animals.
美国FDACFR21规定指的是什么? - 知乎
【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 美国食品药品管理局。 CFR全称是Code of Federal Regulations。 21CFR是《美国联邦法规》 (CFR) 第21条,是有关食品、药品、医疗器械、辐射类电子产品、化妆品、烟草制品的标准。 针对不同的产品在每一个部分都有相关的要求。 具体就是要通过FDA的注册或者达到检测标准。 美国食品安全 …
Code of Federal Regulations - Title 21 - Food and Drugs | FDA
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 of the Code of Federal Regulations - Wikipedia
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 Administration (DEA), and the Office of National Drug Control Policy …
法规解析:什么是 FDA 21 CFR-国外法规-蒲公英 - 制药技术的传 …
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 Part 11的)
Electronic Code of Federal Regulations (e-CFR): Title 21—Food and Drugs
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 (parts 1300 - 1322-1399) chapter iii—office of national drug control policy (parts 1400 - …
21CFR Part 210&211 中英文对照版_2020.4 - 百度文库
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 人采取相应监管措施。
CFR - Code of Federal Regulations Title 21 - Food and Drug Administration
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 formats, see Instructions...