FDA Act definition

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

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, as amended, and the regulations promulgated thereunder, as amended from time to time.

Examples of FDA Act in a sentence

• In case of expired LTO, the following copies may be submitted:(i) expired LTO;(ii) application for renewal; and(iii) Official Receipt as proof of payment of renewal of LTORA 9711, FDA Act of 2009 &its IRR 21.2Additional required documents relevant to the Project that are required by existing laws and/or the Procuring Entity: 1.

• Provided, that the application for renewal was made timely as per DOH AO No. 2016- 003:In case of expired LTO, the following copies may be submitted:(i) expired LTO;(ii) application for renewal; and(iii) Official Receipt as proof of payment of renewal of LTORA 9711, FDA Act of 2009 &its IRR 21.2Additional required documents relevant to the Project that are required by existing laws and/or the Procuring Entity: 1.

• 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 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 Inventory has been stored in compliance with all Laws and is not adulterated or mislabeled, misbranded or unsafe within the meaning of the FDA Act (including the Pesticide and Food Additive Amendment of 1958) and the regulations thereunder.

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 U.S. Federal Food, Drug, and Cosmetic Act.

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

FDA Act means the Food, Drug and Cosmetics Act of 1938, as amended, supplemented or replaced.

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 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).