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
Client Information Package 01/1-01/5
HNCA TAC Client
1. Certification Agreement HNCA-TAC-01/1 (Print, Initial Every Page and Sign)
2. Certification Policy HNCA-TAC-01/2 (Print , Initial Every Page and Sign)
3. Self Labeling SLP-PRO-01/3
4. E-Permit EP-PRO-01/4
5. User Manual Client UMC-DOC-01/5