WHO TRS 863, 1996 Annex 7

WHO TRS (Technical Report Series) 863, 1996 Annex 7

WHO Good Manufacturing Practices: Supplementary Guidelines For The Manufacture Of Investigational Pharmaceutical Products For Clinical Trials in Humans

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TABLE OF CONTENTS

1. Introductory Note

2. General Considerations

3. Glossary

4. Quality Assurance

5. Validation

6. Complaints

7. Recalls

8. Personnel

9. Premises and Equipment

10. Materials

11. Documentation

12. Production

13. Quality Control

14. Shipping, Returns, and Destruction

References

WHO TRS (Technical Report Series) 863, 1996 Annex 7