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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
Certification Agreement- HNCA-TAC-01/1
Kindly read and understand before printing out to sign on the agreement and initial on every page.
Submit the agreement with Certification Policy and other certified relevant documents to HNCA office or any Service Points.
You can choose to submit during your first official application of any services at these locations.