Adverse Event Reporting Guidance for the Medical Device Manufacturer or its Authorized Representative
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(WG2 here is referred to WG4 after the restructuring of work groups.)
Comparison between the GHTF Summary Technical Documentation (STED) formats for Medical Devices and In Vitro Diagnostic Medical Devices and the Common Submission Dossier Template (CSDT) format
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(WG1a here is referred to WG2 after the restructuring of work groups.)
Essential Principles of Safety and Performance of IVD Medical Devices
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(WG1a here is referred to WG2 after the restructuring of work groups.)
AHWP Regulatory Framework for IVD Medical Devices
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(WG1a here is referred to WG2 after the restructuring of work groups.)
Amendment 1 to the GUIDANCE for Member Economy Hosting the Meetings of AHWP or its Technical Committees
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