Categories
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12 Document Control - DCP-DOC-12/1Client Information Package 01/1-01/5ACT 737 & MDR 2012 DocumentsGuidance Document under Medical Device Act 2012 ( Act 737)General Medical Devices (GMD)In-Vitro Diagnostic (IVD) Medical Devices 03 Quality Policy10 Appeals and Disputes11 Complaints HandlingIndustry Engagement & FeedbackUseful Info
General Medical Devices (GMD)
Guidance Documents for General Medical Device Registration
MDAGD0005 Product Grouping for GMD_1st Ed 2013MDAGD0006 Definition of Medical Device_1st Ed 2014MDAGD0007 EPSP for GMD_1st Ed 2014MDAGD0008 CSDT for GMD_1st Ed 2014MDAGD0009 Classification Rules For GMD_1st Ed 2014MDAGD0025 Declaration of Conformity_1st Ed 2016