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This tutorial intends to provide the requirements for placing CE-marked Medical Devices on the European market according to the Regulation (EU) 2017/745 on Medical Devices (MDR). -
The goal of this presentation is to provide you with the essential elements for success and to teach you how to apply the information to your project. Navigating the regulatory process and planning clinical trials can be the most daunting aspect of running your start-up. -
The shortage of personal protective devices has endangered countless lives of healthcare operators working in COVID-19 treatment facilities. This is a widespread and prevalent issue worldwide. After the course, you can take a brief test to receive your certification. Enjoy!
CERTIFIED FOR MEDICAL TRAINING
CLINICAL TRIALS – DIGITAL PLATFORM
INFORMATION SECURITY – MEDICAL EDUCATION
CERTIFIED FOR MEDICAL TRAINING
CLINICAL TRIALS – DIGITAL PLATFORM
INFORMATION SECURITY – MEDICAL EDUCATION
