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 D6.5 Security6.5.1 X6.5.2 X6.5.3 X6.6 Documentation6.6 X X6.7 Ancillary Aspects6.7 X7. Documentation7.1 General Considerations7.1.1 X7.1.2 X7.1.3 X7.1.4 X7.1.5 X7.2 Specifications and Test Procedures7.2.1 X7.2.2 X7.2.3 X X7.3 Test Records7.3.1 X7.3.2 X7.3.3 X7.4 Production Documentation7.4.1 X7.4.2 X7.4.3 X7.4.4 X7.4.5 X7.4.6 X7.4.7 X7.4.8 X7.4.9 X7.4.10 X69
Quality Management System - integrating GMP into ISOISOChapters1 2 3 4 5 6 7 8 9 1011121314151617181920A B C D8. Validation8.1 Validation Policy8.1 X8.2 Preliminary Considerations8.2.1 X8.2.2 X8.3 Qualification8.3.1 X8.3.2 X8.4 Process Validation8.4.1 X8.4.1.1 X8.4.1.2 X8.4.2 X8.4.3 X8.5 Scope8.5.1 X8.5.2 X8.5.3 X8.5.4 X8.6 Validation Documentation8.6.1 X8.6.2 X8.6.3 X8.6.3.1 X8.6.3.2 X8.6.4 X8.6.5 X8.7 Revalidation8.7.1 X8.7.2 X70
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