Participation in the equivalence assessment and determination.

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. Participation in the equivalence assessment and determination.

§ 26.7 Participation in the equivalence assessment and determination.

The authorities listed in appendix B of this subpart will actively participate in these programs to build a sufficient body of evidence for their equivalence determination. Both parties will exercise good faith efforts to complete equivalence assessment as expeditiously as possible to the extent the resources of the authorities allow.

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