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