Medical Device Development
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Medical Device Regulations (MDR) Essentials, A comprehensive guide to EU MDR 2017/745: Classification, GSPR, Clinical Evaluation (CER), and Post-Market Surveillance.
Course Description
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Medical Devices and Regulatory Affairs, Self Learning Course.
Course Description
Overview
A Medical Devices and Regulatory Affairs course is a program of study that covers the regulation ...
Deal
Build a winning strategy for EU MDR Compliance, Our experts will show you how to leverage the benefits of a successful MDR strategy
Course Description
Successful MDR compliance is demonstrated by ...
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ISO 13485:2016 - Awareness on Medical Devices Development, Basic understanding on ISO 13485:2016 International Standard on Design and Development Process in Medical Devices.
Course Description
This ...