Class II Application
Class III Application
Class IV Application
Amendment Form for Class II, III and IV
Medical Device Recall Listings
Medical Device RegulationsMedical Device License ListingQuality Systems 13485/13488Medical Devices Chapter 2 Canadian RequirementsPreparation of Investigational Testing Medical Devices V.3US Food and Drug Administration Device AdviceEU Guidelines – Relating to Medical Devices Directives Medical Devices Guidance Document
Study Group #1 Proposed DocumentsStudy Group # 2 Proposed DocumentsStudy Group # 3 Proposed DocumentsStudy Group # 4 Proposed DocumentsStudy Group # 5 Proposed Documents
Recomendations from the Health Canada Scientific Advisory Panel on Reprocessing of Medical Devices
STED Pilot Program
Quebec centralized ethical review mechanism (English PDF)
Medical Devices Independent Advisory Panel on HPFB Medical Device User Fee Proposal Nov/Dec 2007
