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  1. LII
  2. Electronic Code of Federal Regulations (e-CFR)
  3. Title 21—Food and Drugs
  4. CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  5. SUBCHAPTER A—GENERAL
  6. 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
  7. Subpart C—“Framework” Provisions

21 CFR Part 26 - Subpart C - “Framework” Provisions

  • CFR
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  1. § 26.60 Definitions.
  2. § 26.61 Purpose of this part.
  3. § 26.62 General obligations.
  4. § 26.63 General coverage of this part.
  5. § 26.64 Transitional arrangements.
  6. § 26.65 Designating authorities.
  7. § 26.66 Designation and listing procedures.
  8. § 26.67 Suspension of listed conformity assessment bodies.
  9. § 26.68 Withdrawal of listed conformity assessment bodies.
  10. § 26.69 Monitoring of conformity assessment bodies.
  11. § 26.70 Conformity assessment bodies.
  12. § 26.71 Exchange of information.
  13. § 26.72 Sectoral contact points.
  14. § 26.73 Joint Committee.
  15. § 26.74 Preservation of regulatory authority.
  16. § 26.75 Suspension of recognition obligations.
  17. § 26.76 Confidentiality.
  18. § 26.77 Fees.
  19. § 26.78 Agreements with other countries.
  20. § 26.79 Territorial application.
  21. § 26.80 Entry into force, amendment, and termination.
  22. § 26.81 Final provisions.

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