21 CFR 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
June 25, 2020
§
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
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