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Business · 19/02/2026Updated: 10/16/2026 · 1 min read

Revocation of Regulations Regarding the 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

The FDA is revoking regulations regarding the mutual recognition of pharmaceutical and medical device reports due to being outdated and superseded by newer EU guidelines.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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