e-CFR data is current as of March 4, 2021 |
Title 21 → Chapter I → Subchapter A → Part 26 → Subpart B → §26.44 |
Title 21: Food and Drugs
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
Subpart B—Specific Sector Provisions for Medical Devices
Transmission of product evaluation reports will take place according to the importing party's specified procedures.