Common use of Batch Disposition Clause in Contracts

Batch Disposition. 7.2.1 For each batch, C*P will provide the documentation required in Appendix III. 7.2.2 Certificate of Compliance/Analysis 7.2.2.1 C*P is responsible for ensuring and certifying that the PRODUCTS have been manufactured according to the specifications/procedures documented in the Master Production Records. 7.2.2.2 C*P Qualified Person/QA Representative will sign a Certificate of Compliance confirming that the PRODUCTS have been manufactured, packaged, tested and stored according to the requirements of the Master Production Record and the Drug Product Specification. 7.2.2.3 C*P will provide a Certificate of Analysis indicating the test result from each test performed.