21 CFR Part 226
PART 226—CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES
- PART 226—CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES
- Chapter I—Food and Drug Administration, Department of Health and Human Services › Subchapter C—Drugs: General
- 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.
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