FDA Act definition

FDA Act means the U.S. Federal Food, Drug, and Cosmetic Act, as amended.

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

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).

Examples of FDA Act in a sentence

The Product is not adulterated or misbranded within the meaning of the FDA Act or any similar governmental act or Applicable Law of any jurisdiction.
The Product is not adulterated or misbranded within the meaning of the FDA Act or any similar governmental act or Law of any jurisdiction.
The Company is currently conducting, and has at all times conducted, its business and operations in compliance in all material respects with each applicable Law, including the FDA Act and applicable implementing regulations, orders, policies and guidance issued by the FDA thereunder.
The Existing Products have not been adulterated or misbranded within the meaning of the FDA Act, or within the meaning of any applicable Law.
No Existing Product is or was, at the time of any introduction, an article that is or was prohibited from introduction into interstate commerce under the FDA Act, including Sections 301, 501, 502, 510, 515 or 801 thereof.

More Definitions of FDA Act

FDA Act means the Federal Food, Drug and Cosmetic Act and applicable implementing regulations issued by the FDA, including, as applicable, those requirements relating to the FDA’s current good manufacturing and quality system practices, good laboratory practices and good clinical practices and investigational use.

FDA Act means the Federal Food, Drug, and Cosmetic Act, as amended.

FDA Act means the U.S. Federal Food, Drug, and Cosmetic Act.

FDA Act has the meaning set forth in Section 4.28(a).

FDA Act means the United States Food, Drug and Cosmetic Act and applicable regulations promulgated thereunder.

FDA Act means the Food, Drug and Cosmetics Act of 1938, as amended, supplemented or replaced. “Final Inventory Value” shall have the meaning set forth in Section 2.7(d).

FDA Act means the U.S. Food, Drug and Cosmetic Act of 1938, as amended from time to time, and its Canadian counterpart, the Food and Drugs Act (Canada), as they may be superseded or amended from time to time.