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,
Teachers: Bert Degens,
You will receive a certificate from Mikrocentrum