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  1. LII
  2. Electronic Code of Federal Regulations (e-CFR)
  3. Title 21—Food and Drugs
  4. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  5. SUBCHAPTER C—DRUGS: GENERAL
  6. PART 226—CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES

21 CFR Part 226 - CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES

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  1. Subpart A—General Provisions (§§ 226.1 - 226.10)
  2. Subpart B—Construction and Maintenance of Facilities and Equipment (§§ 226.20 - 226.30)
  3. Subpart C—Product Quality Control (§§ 226.40 - 226.58)
  4. Subpart D—Packaging and Labeling (§ 226.80)
  5. Subpart E—Records and Reports (§§ 226.102 - 226.115)
Authority:
21 U.S.C. 351, 352, 360b, 371, 374.
Source:
40 FR 14031, Mar. 27, 1975, unless otherwise noted.

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