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 § 26.8
21 CFR § 26.8
Other transition activities
June 25, 2020
CFR

As soon as possible, the authorities will jointly determine the essential information which must be present in inspection reports and will cooperate to develop mutually agreed inspection report format(s).

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§ 26.7 Participation in the equivalence assessment and determination
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§ 26.9 Equivalence determination

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