What is the difference between the ISO 13485 certification and the product CE marking?
How to ensure the traceability of my medical device throughout its development cycle?
How to implement a clinical study?
What is the value proposition of my solution? How to segment and quantify my market?
How to finance my solution? What is the reimbursement process for a medical device?
Join the startup accelerator in medical devices of the Brussels Capital Region to obtain answers to these questions and many more!
The Medtech Accelerator helps entrepreneurs develop, challenge and boost the development of their medical device and identify realistic objectives for the continuation of their project through:
Program starts on February 1, 2017.
Program and registration (early-bird registration till December 31, 2016)
More info? Contact Sophie.