​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 or 2 days
MMD-102     ISO 13485:2016 Internal Auditor Training​   Find out more	​2 days
MMD-103     Understanding the US FDA Medical Device   ​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     Medical Device Root Cause Analysis and CAPA​​   ​Find out more	2 days
MMD-108     US FDA Inspection Readiness​   ​Find out more	2 days
MMD-109     Awareness on the Medical Device Single Audit Program (MDSAP)​   ​Find out more	1 or 2 days
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
MMD-113     An Overview of Medical Device GMP requirements for South Korea   ​Find out more	1 day
MMD-114     ​Understanding the EU Medical Device Regulation 2017/745   ​Find out more	2 or 3days
MMD-115     ​Internal Auditor Training based on US FDA CFR Title 21 Part 820   ​Find out more	2 days
MMD-116     ​Overview of Brazilian GMP for Medical Devices & IVD’s (RDC 665/2022)   ​​Find out more	2 days
MMD-117    Integrating ISO 13485:2016 with 21 CFR Part 820 – Navigating the FDA’s Quality Management                       System Regulation (QMSR)   ​​​Find out more	2 days
MMD-118     ​Introduction to ISO 11607: Packaging for Terminally Sterilized Medical Devices   ​​​​Find out more	1 day
MMD-119    ​An Overview of GMP requirements for Brazil and South Korea   ​​​Find out more	3 days
MMD-120    Understanding MHLW Ministerial Ordinance No. 169 (Japan) – Quality Management System for ​                      Medical Devices   Find out more	1 day
MMD-121     ​Understanding Good Distribution Practice (GDP) for Pharmaceutical & Medical Device Supply ​                       Chain   Find out more	1 day
MMD-122     ISO 13485:2016, Medical Device Single Audit Program (MDSAP), Medical Device Regulation ​                       (MDR) Internal Auditor Training   Find out more	2 days
MMD-123     Computer Software Validation (CSV) & Data Integrity for Medical Devices - GAMP 5 & Regulatory ​                       Compliance   ​Find out more	2 days
MMD-124     ​An Overview of Good Distribution Practice for Medical Devices (GDPMD)   ​Find out more	1 day
MMD-125     Understanding of MS 2058:2018 Good Engineering Maintenance Management of Active Medical                        Devices   Find out more	1 day
MMD-126     ​Understanding of Medical Devices Regulations (SOR/98-282)   ​Find out more	1 day
MMD-127     ​Understanding of US FDA Quality Management System Regulation   ​Find out more	2 days

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