Martin de Bruin, MSc, MBA
At Qserve Martin is responsible for the commercial activities, including the launch of the first MDR-app. Together with Gert Bos he drives the roadmap to EU-MDR implementation, where medical device manufacturers around Europe follow a monthly workshop to get trained on the EU-MDR.
Martin has 23 years experience in pharma and medical devices, as product manager, auditor, technical reviewer, sales and account manager.
Martin holds a degree in polymer chemistry, he has dealt as Notified Body technical reviewer & auditor with a large range of devices mostly in the non-active device area (leads, implants, borderline products), in cardiovascular, ophthalmic and wound care fields.
He also holds a MBA, focus on marketing, and he has executed this combination in various marketing & technical sales roles. Martin combines knowledge of regulations worldwide with pragmatic sales and account management.