Chapter 15 - Current Good Manufacturing Practices in the Manufacture of Drugs
- Section VI-1501 - Definitions [formerly paragraph 6:191]
- Section VI-1503 - Permits [formerly paragraph 6:192]
- Section VI-1505 - Public Display of Permits [formerly part of paragraph 6:192]
- Section VI-1507 - Permit Exemptions [formerly paragraph 6:193]
- Section VI-1509 - Examination, Condemnation and Destruction of Unwholesome or Adulterated Drugs [formerly paragraph 6:194]
- Section VI-1511 - Personnel [formerly paragraph 6:195]
- Section VI-1513 - Building Construction [formerly paragraph 6:197]
- Section VI-1515 - Building Requirements [formerly paragraph 6:198-1]
- Section VI-1517 - Equipment [formerly paragraph 6:199]
- Section VI-1519 - Product Production and Quality Control [formerly paragraph 6:200]
- Section VI-1521 - Components [formerly paragraph 6:202]
- Section VI-1523 - Product Containers and Their Components [formerly paragraph 6:203]
- Section VI-1525 - Laboratory Controls [formerly paragraph 6:204]
- Section VI-1527 - Stability [formerly paragraph 6:206]
- Section VI-1529 - Expiration Dating [formerly paragraph 6:207]
- Section VI-1531 - Packaging and Labeling [formerly paragraph 6:208]
- Section VI-1533 - Records and Reports [formerly paragraph 6:209-1]
- Section VI-1535 - Distribution Records [formerly paragraph 6:209-3]
- Section VI-1537 - Complaint Files [formerly paragraph 6:210]