Manufacturing and Equipment Data. Bachem shall be responsible for keeping records of equipment usage, cleaning, raw material batch numbers and certification as well as in process results and parameters. Such documentation shall be retained by Bachem as described in Section 6.9 hereunder.
Manufacturing and Equipment Data. 5.9.1 C*P is responsible for keeping records of equipment usage (previous PRODUCT produced is non-dedicated equipment), cleaning, and any maintenance/calibration performed.
Manufacturing and Equipment Data. Sanofi or its subcontractor shall be responsible for keeping their records in accordance with cGMP as defined in Section 4.8 of the Sanofi Internal Quality Agreement.
Manufacturing and Equipment Data. 5.9.1 Xxxxxx is responsible for keeping records of equipment usage (previous product produced in non-dedicated equipment), cleaning, and any maintenance/calibration performed.
Manufacturing and Equipment Data. SUPPLIER is responsible for safe keeping and retention of records of machine usage (previous Products produced in non-dedicated machinery), cleaning, any maintenance/calibration performed, Raw Material/Chemical Component batch/lot numbers and certification, in-process results/parameters, and test results and shall perform all functions in accordance with regulatory requirements.
Manufacturing and Equipment Data. SkyePharma is responsible for keeping records of equipment usage (previous PRODUCT produced in non-dedicated equipment), cleaning and any maintenance and/or calibration performed.
Manufacturing and Equipment Data. Seller is responsible for keeping records of equipment usage, raw materials batch numbers and certification, in process results and parameters, and previous Products used in equipment if non-dedicated equipment is used.
Manufacturing and Equipment Data. 5 5.11 STORAGE AND SHIPMENT........................................5 6. QUALITY CONTROL....................................................6 6.1 GENERAL.....................................................6 6.2 IN-PROCESS AND PRODUCT TESTING..............................6
Manufacturing and Equipment Data. ORPHAN, CELLTECH, and any contract manufacturer is responsible for keeping records of equipment usage (in case of using non-dedicated equipment), cleaning, any maintenance/calibration performed, batch records and laboratories raw data as appropriate for their facilities and equipment. QUALITY AGREEMENT APPENDIX: PAGE 4
Manufacturing and Equipment Data
