cGMP. “cGMP” means those practices in the manufacture of pharmaceutical products that are recognized as the current good manufacturing practices by the FDA in accordance with FDA regulations, guidelines, other administrative interpretations, and rulings in connection therewith, including but not limited to those regulations cited in 21 C.F.R. parts 210 and 211, all as they may be amended from time to time.
Appears in 4 contracts
Samples: Pharmaceutical Manufacturing and Exclusive Supply Agreement, Three Way Agreement, Pharmaceutical Manufacturing and Exclusive Supply Agreement (Nabriva Therapeutics PLC)
