Title 21

PART 226

Part 226 - Current Good Manufacturing Practice For Type A Medicated Articles

PART 226 - CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES Authority:21 U.S.C. 351, 352, 360b, 371, 374. Source:40 FR 14031, Mar. 27, 1975, unless otherwise noted.

21:4.0.1.1.15.1SUBPART A
Subpart A - General Provisions
21:4.0.1.1.15.1.1.1SECTION 226.1
   226.1 Current good manufacturing practice.
21:4.0.1.1.15.1.1.2SECTION 226.10
   226.10 Personnel.
21:4.0.1.1.15.2SUBPART B
Subpart B - Construction and Maintenance of Facilities and Equipment
21:4.0.1.1.15.2.1.1SECTION 226.20
   226.20 Buildings.
21:4.0.1.1.15.2.1.2SECTION 226.30
   226.30 Equipment.
21:4.0.1.1.15.3SUBPART C
Subpart C - Product Quality Control
21:4.0.1.1.15.3.1.1SECTION 226.40
   226.40 Production and control procedures.
21:4.0.1.1.15.3.1.2SECTION 226.42
   226.42 Components.
21:4.0.1.1.15.3.1.3SECTION 226.58
   226.58 Laboratory controls.
21:4.0.1.1.15.4SUBPART D
Subpart D - Packaging and Labeling
21:4.0.1.1.15.4.1.1SECTION 226.80
   226.80 Packaging and labeling.
21:4.0.1.1.15.5SUBPART E
Subpart E - Records and Reports
21:4.0.1.1.15.5.1.1SECTION 226.102
   226.102 Master-formula and batch-production records.
21:4.0.1.1.15.5.1.2SECTION 226.110
   226.110 Distribution records.
21:4.0.1.1.15.5.1.3SECTION 226.115
   226.115 Complaint files.