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 B - Specific Sector Provisions for Medical Devices
  7. 21 CFR § 26.45
21 CFR § 26.45
Monitoring continued equivalence
June 25, 2020
CFR

Monitoring activities will be carried out in accordance with §26.69.

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§ 26.44 Transmission of product evaluation reports
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§ 26.46 Listing of additional CAB's

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