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Pages in category "Pharmaceutical regulation in the United States" The following 15 pages are in this category, out of 15 total. This list may not reflect recent changes .
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 (ONDCP). [1] It is divided into three chapters: Chapter I — Food and Drug Administration
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.
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Pharmaceutical regulation in the United States (15 P) Pages in category "Pharmaceuticals policy" The following 143 pages are in this category, out of 143 total.
UNITED STATES SECURITIES AND EXCHANGE COMMISSION Washington, D.C. 20549 FORM 10-K ANNUAL REPORT PURSUANT TO SECTION 13 OF THE SECURITIES EXCHANGE ACT OF 1934 For the fiscal year ended January 3, 2010 JOHNSON & JOHNSON (Exact name of registrant as specified in its charter) Registrant’s telephone number, including area code: (732) 524-0400
Pharmaceutical regulation in the United States (15 P) Pages in category "Drug policy of the United States" The following 77 pages are in this category, out of 77 total.
The regulation of therapeutic goods, defined as drugs and therapeutic devices, varies by jurisdiction. In some countries, such as the United States, they are regulated at the national level by a single agency. In other jurisdictions they are regulated at the state level, or at both state and national levels by various bodies, as in Australia.