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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter C - Drugs: General |
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Part 226 - Current Good Manufacturing Practice for Type a Medicated Articles |
| Subpart A - General Provisions |
| § 226.1 - Current good manufacturing practice. |
| § 226.10 - Personnel. |
| Subpart B - Construction and Maintenance of Facilities and Equipment |
| § 226.20 - Buildings. |
| § 226.30 - Equipment. |
| Subpart C - Product Quality Control |
| § 226.40 - Production and control procedures. |
| § 226.42 - Components. |
| § 226.58 - Laboratory controls. |
| Subpart D - Packaging and Labeling |
| § 226.80 - Packaging and labeling. |
| Subpart E - Records and Reports |
| § 226.102 - Master-formula and batch-production records. |
| § 226.110 - Distribution records. |
| § 226.115 - Complaint files. |