Medical Devices Course: CE marking and FDA approval pathways 

In this 2.5 days course you will learn everything about CE marking and FDA approval pathways for new medical devices. You will know how to plan, set-up and execute development pathways and are familiar with demands and regulations.

Date: 3-4-5 April (FULL) and 9-10-11 October

Location: Brightlands Chemelot Campus,
Center Court

Teachers: Bert Degens,
Mikrocentrum


You will receive a certificate from Mikrocentrum

Medical Devices Course: CE marking and FDA

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