PART 26—MUTUAL RECOGNITION OF PHARMACEUTICAL GOOD MANUFACTURING PRACTICE REPORTS, MEDICAL DEVICE QUALITY SYSTEM AUDIT REPORTS, AND CERTAIN MEDICAL DEVICE PRODUCT EVALUATION REPORTS: UNITED STAT
- 26.0—General.
- SUBPART A—Specific Sector Provisions for Pharmaceutical Good Manufacturing Practices (§26.1 to §26.21)
- SUBPART B—Specific Sector Provisions for Medical Devices (§26.31 to §26.50)
- SUBPART C—“Framework” Provisions (§26.60 to §26.81)