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Quality Management System

Quality Management System (QMS) for Active Pharmaceutical Ingredients (API) Manufacturers integrating GMP (ICH Q7a) into ISO (9001: 2000) September 2005 APIC / CEFIC Quality Management System - integrating GMP (ICH Q7a) into ISO (9001: 2000) Page 2 of 73 Table of Contents I. Introduction II. Objective and Scope III. Quality Management Systems for API manufacturers 1. Quality Management System 2. Management responsibility 3. Resource Management 4. Product realization (Manufacturing Operations) 5. Measurement, analysis and improvement (Evaluation Activities) IV. Supplementary Information 1. Identification of System approaches in Q7a 2. Description of processes 3. Structure of a Quality manual 4. Cross- reference of APIC QMS documents (from old to new ) 5. Assistance for implementation of a QMS 6. Matrix GMP(Q7a) / ISO (9001:2000) V. Glossary VI. Abbreviations VII.

3. Structure of a Quality Manual 4. Cross-reference of APIC QMS documents (from “old” to “new”) 5. Assistance for implementation of a QMS 6. Matrix GMP(Q7a) / ISO (9001:2000) V. Glossary VI. Abbreviations VII. References VIII. Acknowledgements

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