Common use of FD&C Act Clause in Contracts

FD&C Act. “FD&C Act” shall mean the United States Federal Food, Drug and Cosmetic Act, as amended.

Appears in 6 contracts

Sources: Pharmaceutical Product Supply Agreement, Pharmaceutical Manufacturing and Exclusive Supply Agreement (Nabriva Therapeutics PLC), Commercial Supply Agreement (BioPharmX Corp)

FD&C Act. “FD&C Act” shall mean the United States Federal Food, Drug Drug, and Cosmetic Act, as amended, and the rules and regulations promulgated thereunder.

Appears in 1 contract

Sources: Development and License Agreement (SCOLR Pharma, Inc.)

FD&C Act. “FD&C Act” shall mean the United States Federal Food, Drug Drug, and Cosmetic ActAct (21 U.S.C. § 301 et seq.), as amended, and the rules and regulations promulgated thereunder.

Appears in 1 contract

Sources: Development and Commercialization Agreement (Advanced Life Sciences Holdings, Inc.)

FD&C Act. “FD&C Act” shall mean the United States Federal Food, Drug Drug, and Cosmetic Act, as amendedamended from time to time, and the rules and regulations promulgated thereunder.

Appears in 1 contract

Sources: License Agreement (Inovio Biomedical Corp)

FD&C Act. “FD&C Act” shall mean the United States Federal Food, Drug and Cosmetic Act, 21 U.S.C. § 301 et seq., as amendedamended from time to time, together with any rules, regulations and requirements promulgated thereunder (including all additions, supplements, extensions, and modifications thereto).

Appears in 1 contract

Sources: Pharmaceutical Manufacturing and Supply Agreement (Omeros Corp)

FD&C Act. “FD&C Act” shall mean means the United States Federal Food, Drug and Cosmetic Act, as amendedamended from time to time.

Appears in 1 contract

Sources: Three Way Agreement (Nabriva Therapeutics PLC)