Code of Federal Regulations · Subpart
Subpart B — Specific Sector Provisions For Medical Devices
21 C.F.R. pt. 26, subpt. B
- § 26.31 Purpose
- § 26.32 Scope
- § 26.33 Product Coverage
- § 26.34 Regulatory Authorities
- § 26.35 Length And Purpose Of Transition Period
- § 26.36 Listing Of Cab's
- § 26.37 Confidence Building Activities
- § 26.38 Other Transition Period Activities
- § 26.39 Equivalence Assessment
- § 26.40 Start Of The Operational Period
- § 26.41 Exchange And Endorsement Of Quality System Evaluation Reports
- § 26.42 Exchange And Endorsement Of Product Evaluation Reports
- § 26.43 Transmission Of Quality System Evaluation Reports
- § 26.44 Transmission Of Product Evaluation Reports
- § 26.45 Monitoring Continued Equivalence
- § 26.46 Listing Of Additional Cab's
- § 26.47 Role And Composition Of The Joint Sectoral Committee
- § 26.48 Harmonization
- § 26.49 Regulatory Cooperation
- § 26.50 Alert System And Exchange Of Postmarket Vigilance Reports