Page:United States Statutes at Large Volume 124.djvu/1090 - Wikisource, the free online library
Referencing the Definition of “Device” in the Federal Food, Drug, and Cosmetic Act in Guidance, Regulatory Documents, Commun
According to the Federal Food, Drug, and Cosmetic Act, as amended, Section 201 (g) (1), the term “DRUG” is defined to mean:
eCFR :: 21 CFR Part 201 -- Labeling
GRAS: Gain US Market Access
An Overview of The Cures Acceleration Network - April 2010
FDA Issues Draft Guidance to Clarify Referencing of the Terms “Device” and “Counterfeit Device”
FDA ALERT
PUBLIC LAW 87-781-.OCT. 10,1962 Public Law 87-781 ^ Be it enacted hy the Seriate and House of Representatives of the United Stat
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ACTION: Revised DATE: 08/06/2008 3:57 PM
Nutritional informed consent
Page:United States Statutes at Large Volume 76.djvu/828 - Wikisource, the free online library
Page 25 TITLE 21—FOOD AND DRUGS § 214. Previous laws unaffected Nothing in this chapter shall be construed as modifying or re
b) (4)
Subtitle B--Federal Trade Commission Review As amended by “Patient Right to Know Drug Prices Act” (Public Law No. 115-263)
H. R. 3303
Ohio Administrative Code
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135 PART 207—REQUIREMENTS FOR FOREIGN AND DOMESTIC ESTAB- LISHMENT REGISTRATION AND LISTING FOR HUMAN DRUGS, IN- CLUDING DRUGS
Act of June 25, 1938 (Federal Food, Drug, and Cosmetic Act), Public Law 75-717, 52 STAT 1040, which prohibited the movement in interstate commerce of adulterated and misbranded food, drugs, devices, and cosmetics
Food and Drug Administration, HHS § 369.9
Everything You Need to Know About The Food Drug and Cosmetic Act
150 PART 208—MEDICATION GUIDES FOR PRESCRIPTION DRUG PROD- UCTS Subpart A—General Provisions
