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e-CFR data is current as of October 22, 2020

Title 21Chapter ISubchapter CPart 226


TITLE 21—Food and Drugs

CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

SUBCHAPTER C—DRUGS: GENERAL

PART 226—CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES

rule

Subpart A—GENERAL PROVISIONS

§226.1
Current good manufacturing practice.
§226.10
Personnel.
rule

Subpart B—CONSTRUCTION AND MAINTENANCE OF FACILITIES AND EQUIPMENT

§226.20
Buildings.
§226.30
Equipment.
rule

Subpart C—PRODUCT QUALITY CONTROL

§226.40
Production and control procedures.
§226.42
Components.
§226.58
Laboratory controls.
rule

Subpart D—PACKAGING AND LABELING

§226.80
Packaging and labeling.
rule

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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