FDA Act definition

FDA Act means the U.S. Federal Food, Drug, and Cosmetic Act, as amended.
FDA Act means the Federal Food, Drug and Cosmetic Act, as amended.
FDA Act means the United States Federal Food, Drug, and Cosmetic Act of 1938, as amended.

Examples of FDA Act in a sentence

  • All Acquired Regulatory Approvals and all related records (e.g., the Regulatory Documentation) have been maintained in all material respects in accordance with all applicable Laws, including the FDA Act.

  • Seller’s use of the Acquired Assets, Acquired Regulatory Approvals and Licensed Intellectual Property is being, and for the past [***] has been, conducted in compliance in all material respects with the Acquired Regulatory Approvals and all applicable Laws, including the FDA Act.


More Definitions of FDA Act

FDA Act means the U.S. Food, Drug and Cosmetic Act of 1938, as it may be superseded or amended from time to time.
FDA Act means the United States Federal Food, Drug, and Cosmetic Act, 21 U.S.C. § 301 et seq., as amended from time to time, together with any rules, regulations and requirements promulgated thereunder (including all additions, supplements, extensions, and modifications thereto).
FDA Act means the United States Food, Drug and Cosmetic Act, as amended, and applicable regulations and guidances thereunder.
FDA Act means the Food, Drug and Cosmetics Act of 1938, as amended, supplemented or replaced.