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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 211. CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
  7. Subpart E. Control of Components and Drug Product Containers and Closures

21 CFR Subpart E - Control of Components and Drug Product Containers and Closures

  • CFR
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  1. § 211.80 General requirements.
  2. § 211.82 Receipt and storage of untested components, drug product containers, and closures.
  3. § 211.84 Testing and approval or rejection of components, drug product containers, and closures.
  4. § 211.86 Use of approved components, drug product containers, and closures.
  5. § 211.87 Retesting of approved components, drug product containers, and closures.
  6. § 211.89 Rejected components, drug product containers, and closures.
  7. § 211.94 Drug product containers and closures.

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