​ISO 13485 Quality Management for Medical Devices       

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MMD-101      Understanding the Requirements of ISO 13485:2016 Quality Management System for Medical ​                        Devices   Find out more	1 day
MMD-102      ISO 13485:2016 Internal Auditor Training​   Find out more	​2 days
MMD-103      ​Understanding of USFDA CFR Title 21 Part 820 Quality System Regulation   ​Find out more	2 days
MMD-104      ​EU Medical Device Clinical Evaluation​   ​Find out more	2 days
MMD-105     Understanding the Requirements of ISO 14971:2019 – Risk Based Thinking   ​Find out more	2 days
MMD-106     ​Validation Process Training for Medical Devices   ​Find out more	1 day
MMD-107     ETO Validation Process​   ​Find out more	1 day
MMD-108     US FDA Inspection Readiness​   ​Find out more	2 days
MMD-109     Management Overview on Medical Device Single Audit Program (MDSAP)​   ​Find out more	1 day
MMD-110     Medical Device Single Audit Program (MDSAP) Internal Auditor Training    ​Find out more	2 days
MMD-111     An Overview of 21 CFR 820 & US FDA's Medical Device cGMP    ​Find out more	​2 days
MMD-112     An Overview of 21 Japanese Pharmaceuticals & Medical Device Laws    ​Find out more	​2 days

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