2024 AMMI Training Wishlist

2024 Training Wish List
You are invited to submit your 2024 training wish list and we will turn the most requested courses into public training classes for you!
Name
Position
Company
Work email
Please click your preferred training mode
Choose from drop down menu.
My training wish list in 2024

ISO13485 QMSISO13485 Internal AuditUS FDA 21 CFR Part 820 QSRISO14971 Risk ManagementProcess ValidationSoftware Validation Requirements and Excel 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 RequirementsJapanese 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 Certification Programme

Medtech Quality Professional Course (22 days)Medtech Regulatory Compliance Course (10 days)Medtech Manufacturing Excellence Course (21 days)AMMI-Universiti Malaysia Perlis (UniMAP) Professional Certificate in Medical Device Manufacturing (8 days)
Please type the training wish list not listed above
Should be Empty:

2024 Training Wish List