Medical Devices Course: Design Control & Risk Management

Obtaining regulatory approval for medical devices is a complicated challenge. For everybody working on the development of medical devices it is essential to obtain awareness and knowledge about regulatory pathways and demands for medical devices and quality systems. 

This 2 day course builds awareness and focuses on (further) developing your skills on how to apply and hence cover the design control and risk management requirements with regards to medical devices for the EU and US markets. It is mandatory to first follow the training on regulatory pathways applying to medical devices with regards to the EU and US market (CE Marking and FDA Approval). 

Date: 3 & 4 November 

Location: Brightlands Chemelot Campus

Teacher: Bert Degens
Mikrocentrum

You will receive a certificate from Mikrocentrum.