Monitoring continued equivalence.

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. General
  6. 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
  7. Specific Sector Provisions for Medical Devices
  8. Monitoring continued equivalence.

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§ 26.45 Monitoring continued equivalence.

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


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