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The CFR Title 21 Parts 11, 210, 211, 820 Memory Jogger
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Table of Contents
ISBN
1. Table of Contents: Part 11
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2. Subpart A - General Provisions
3. Subpart B - Electronic Records
4. Subpart C - Electronic Signatures
5. Guidance for Industry
6. PART 210 - CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
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7. PART 211 - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
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8. Subpart A - General Provisions
9. Subpart B - Organization and Personnel
10. Subpart C - Buildings and Facilities
11. Subpart D - Equipment
12. Subpart E - Control of Components and Drug Product Containers and Closures
13. Subpart F - Production and Process Controls
14. Subpart G - Packaging and Labeling Control
15. Subpart H - Holding and Distribution
16. Subpart I - Laboratory Controls
17. Subpart J - Records and Reports
18. Subpart K - Returned and Salvaged Drug Products
19. Table of Contents: Part 820
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20. Subpart A - General Provisions
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21. Subpart B - Quality System Requirements
22. Subpart C - Design Controls
23. Subpart D - Document Controls
24. Subpart E - Purchasing Controls
25. Subpart F - Identification and Traceability
26. Subpart G - Production and Process Controls
27. Subpart H - Acceptance Activities
28. Subpart I - Nonconforming Product
29. Subpart J - Corrective and Preventive Action
30. Subpart K - Labeling and Package Control
31. Subpart L - Handling, Storage, Distribution, and Installation
32. Subpart M - Records
33. Subpart N - Servicing
34. Subpart O - Statistical Techniques