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U.S. Code of Federal Regulations
Regulations most recently checked for updates: Aug 28, 2025
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Title 21
Chapter I
Part 26 - 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
§ 26.0 - General.
Subpart A [§ 26.1 - § 26.21] - Subpart A—Specific Sector Provisions for Pharmaceutical Good Manufacturing Practices
Subpart B [§ 26.31 - § 26.50] - Subpart B—Specific Sector Provisions for Medical Devices
Subpart C [§ 26.60 - § 26.81] - Subpart C—“Framework” Provisions
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