2025 AMMI Training Wishlist

2025 Training Wish List
You are invited to submit your 2025 training wish list and we will turn the most requested courses into public training classes for you!
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My training wish list in 2025

ISO13485 QMSISO13485 Internal AuditUS FDA 21 CFR Part 820 QSRISO14971 Risk ManagementProcess ValidationSoftware Validation RequirementsExcel Spreadsheet ValidationTest Method ValidationDesign ControlChange ControlISO10993 Biological EvaluationMedical Device Usability/Human Factor EngineeringEtO SterilizationGamma SterilizationMedical Device PackagingCleanroom and Associated Control Environment (ISO14644 & ISO14698)Medical Device Single Audit Program (MDSAP)EU Medical Device Regulation (EU MDR)EU In-Vitro Diagnostic Regulations (EU IVDR)US FDA Premarket Requirements (510k)Japanese Pharmaceutical and Medical Device Act (PMDA)Malaysia Good Distribution Practice for Medical Device (GDPMD)GDPMD Internal AuditOverview of the Global Medical Device Regulatory System & Medical Device ClassificationLabelling of Medical Devices (ISO15223-1)Good Documentation PracticesNCR/CAPA/Complaint HandlingPost Market Surveillance, Vigilance and Adverse Event InvestigationEffective Root Cause AnalysisAcceptance Sampling MethodFailure Modes and Effects Analysis (FMEA)Statistical Process ControlStatistical Hypothesis TestingMeasurement System AnalysisProcess Mapping & AnalysisDesign of ExperimentsSupply Chain Management (Medical Device Industry)Supplier Audit Training (Medical Device Industry)
AMMI Medtech Professional Certification Programme

Manufacturing Excellence (10 days)Quality Assurance (10 days)Regulatory Affairs (8 days)Production (6 days) (for manufacturing supervisors)
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2025 Training Wish List