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.

• Authority: 21 U.S.C. 351, 352, 360b, 371, 374.
• Source: 40 FR 14031, Mar. 27, 1975, unless otherwise noted.

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

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