Appendixes C-F to Subpart B of Part 26 - [Reserved], Subpart B - Specific Sector Provisions for Medical Devices, 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, SubChapter A - General, Chapter I - Food and Drug Administration, Department of Health and Human Services, Title 21 - Food and Drugs, Code of Federal Regulations

99-8199. Final rule; correction. 99-8199. Mutual Recognition of Pharmaceutical Good Manufacturing Practice Inspection Reports, Medical Device Quality System Audit Reports, and Certain Medical Device Product Evaluation Reports Between the United States and the European Community; Correction
98-29609. Final rule. 98-29609. Mutual Recognition of Pharmaceutical Good Manufacturing Practice Inspection Reports, Medical Device Quality System Audit Reports, and Certain Medical Device Product Evaluation Reports Between the United States and the European Community
98-9486. Proposed rule. 98-9486. Mutual Recognition of the Food and Drug Administration and European Community Member State Conformity Assessment Procedures; Pharmaceutical GMP Inspection Reports, Medical Device Quality System Evaluation Reports, and Certain Medical Device Premarket Evaluation Reports