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Code of Federal Regulations (Last Updated: November 8, 2024)

Title 21 - Food and Drugs

Chapter I - Food and Drug Administration, Department of Health and Human Services

SubChapter A - General

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

Subpart B - Specific Sector Provisions for Medical Devices

§ 26.45 - Monitoring continued equivalence.

Latest version.

§ 26.45 Monitoring continued equivalence.

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

                    
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