Quality Management System for Active pharmaceutical

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Quality Management System - integrating GMP into ISOISOChapters1 2 3 4 5 6 7 8 9 1011121314151617181920A B C D9. Change Control9.1 Change Control Procedures9.1.1 X9.1.2 X9.1.3 X9.2 Implementation of Changes9.2.1 X9.2.2 X10. Contract Manufacture or Analysis10.1 Contract10.1.1 X10.1.2 X11. Materials Management11.1 Purchasing and Control11.1.1 X11.1.2 X11.1.3 X11.1.4 X11.2 Receipt and Quarantine of Materials11.2.1 X11.2.2 X11.2.3 X11.2.4 X11.2.5 X11.2.6 X X11.2.7 X11.2.8 X11.2.9 X X X11.3 Issuing or Distribution of Materials11.3.1 X11.3.2 X11.3.3 XISOChapters1 2 3 4 5 6 7 8 9 1011121314151617181920A B C D71
Quality Management System - integrating GMP into ISOISOChapters1 2 3 4 5 6 7 8 9 1011121314151617181920A B C D11.4 Specific Management of API.11.4.1 X11.4.2 X11.4.3 X12. Sampling12.1 Facilities for Sampling12.1.1 X12.1.2 X12.2 Sampling Procedures12.2.1 X12.2.2 X12.2.3 X12.2.4 X12.2.5 X12.2.6 X12.2.7 X13. Filling and Labelling of API13.1 Packaging Materials13.1.2 X13.2 Filling/Packaging13.2.1 X13.2.2 X13.2.3 X13.2.4 X13.3 Labels and Labelling13.3.1 X13.3.2 X13.3.3 X13.3.4 X13.3.5 X72
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