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
In section 2— (1) redesignate subsections (d) and (e) as sub- sections (e) and (f), respectively; and (2) insert after subsect
Guidance for Industry and FDA Staff:
The Safety Assessment and Regulatory Authority to Use Flavors – Focus on E-Cigarettes First posted May, 2013 Revised March 3,
Accompanying Such Article
Food and Drug Administration, HHS § 369.9
An Overview of The Cures Acceleration Network - April 2010
135 PART 207—REQUIREMENTS FOR FOREIGN AND DOMESTIC ESTAB- LISHMENT REGISTRATION AND LISTING FOR HUMAN DRUGS, IN- CLUDING DRUGS
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
S. 735
Safety Assessment and Regulatory Authority to Use: Focus on ENDS and Flavored Tobacco Products
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Page:United States Statutes at Large Volume 76.djvu/828 - Wikisource, the free online library
GRAS: Gain US Market Access
Food and Drug Administration, HHS § 117.3
ACTION: Revised DATE: 08/06/2008 3:57 PM
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
FDA Issues Draft Guidance to Clarify Referencing of the Terms “Device” and “Counterfeit Device”
