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The CFR Title 21 Parts 210 & 211 Memory Jogger
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Table of Contents
ISBN
1. PART 210 - CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PROCESSING, PACKING, OR HOLDING OF DRUGS; GENERAL
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2. PART 211 - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
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3. Subpart A - General Provisions
4. Subpart B - Organization and Personnel
5. Subpart C - Buildings and Facilities
6. Subpart D - Equipment
7. Subpart E - Control of Components and Drug Product Containers and Closures
8. Subpart F - Production and Process Controls
9. Subpart G - Packaging and Labeling Control
10. Subpart H - Holding and Distribution
11. Subpart I - Laboratory Controls
12. Subpart J - Records and Reports
13. Subpart K - Returned and Salvaged Drug Products