21 CFR Part 225
PART 225—CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS
- PART 225—CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS
- Chapter I—Food and Drug Administration, Department of Health and Human Services › Subchapter C—Drugs: General
- Subpart A—General Provisions
- § 225.1 Current good manufacturing practice.
- § 225.10 Personnel.
- Subpart B—Construction and Maintenance of Facilities and Equipment
- § 225.20 Buildings.
- § 225.30 Equipment.
- § 225.35 Use of work areas, equipment, and storage areas for other manufacturing and storage purpose.
- Subpart C—Product Quality Control
- § 225.42 Components.
- § 225.58 Laboratory controls.
- § 225.65 Equipment cleanout procedures.
- Subpart D—Packaging and Labeling
- § 225.80 Labeling.
- Subpart E—Records and Reports
- § 225.102 Master record file and production records.
- § 225.110 Distribution records.
- § 225.115 Complaint files.
- Subpart F—Facilities and Equipment
- § 225.120 Buildings and grounds.
- § 225.130 Equipment.
- § 225.135 Work and storage areas.
- Subpart G—Product Quality Assurance
- § 225.142 Components.
- § 225.158 Laboratory assays.
- § 225.165 Equipment cleanout procedures.
- Subpart H—Labeling
- § 225.180 Labeling.
- Subpart I—Records
- § 225.202 Formula, production, and distribution records.
Feedback