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 Pharmaceutical Good Manufacturing Practices
8. Monitoring continued equivalence.

§ 26.15 Monitoring continued equivalence.

Monitoring activities for the purpose of maintaining equivalence shall include review of the exchange of inspection reports and their quality and timeliness; performance of a limited number of joint inspections; and the conduct of common training sessions.

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