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 |
2 days |
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2 days |
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2 days |
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2 days |
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