Code of Federal Regulations · Part

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

21 C.F.R. pt. 26

• § 26.0 General
• Subpart A Specific Sector Provisions For Pharmaceutical Good Manufacturing Practices
• Subpart B Specific Sector Provisions For Medical Devices
• Subpart C “framework” Provisions