1. LawStack
  2. Title 21 - Food and Drugs
  3. Chapter I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  4. Subchapter A - GENERAL
  5. Part 26 - MUTUAL RECOGNITION OF PHARMACEUTICAL GOOD MANUFACTURING PRACTICE REPORTS, MEDICAL DEVICE QUALITY SYSTEM AUDIT REPORTS, AND CERTAIN MEDICAL DEVICE PRODUCT EVALUATION REPORTS: UNITED STATES AND THE EUROPEAN COMMUNITY
  6. Subpart A - Specific Sector Provisions for Pharmaceutical Good Manufacturing Practices
  7. 21 CFR § 26.5
21 CFR § 26.5
Length of transition period
June 25, 2020
CFR

A 3-year transition period will start immediately after the effective date described in §26.80(a).

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§ 26.4 Product coverage
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§ 26.6 Equivalence assessment

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