Master Batch Record. (MBR) shall mean the formal set of instructions setting forth the procedure to be followed for the Production of Drug Product, including but not limited to the history of a Batch from the raw material stage up through and until completion of the Batch, a complete list of all active and inactive ingredients, components, weights and measures, descriptions of Drug Product containers, closures, packaging materials, and labeling and complete specifications for each.
Appears in 2 contracts
Sources: Drug Product Development and Clinical Supply Agreement, Drug Product Development and Clinical Supply Agreement (Nuvelo Inc)