Dipl.-Ing. Delvyn Heinsch has been active in the health sciences sector for over 13 years. Since 2019, he has been supporting global clients as a qtec expert on regulatory topics such as the successful market approval of medical devices and in vitro diagnostic medical devices (IVDs).
As General Manager of qtec EuRep, he helps international manufacturers gain access to the European market.
Delvyn Heinsch conducts training sessions for qtec Academy, DIN Academy, and Vorest AG, educating medical device manufacturers, pharmaceutical companies, authorities, and Notified Bodies on a wide range of topics in the medical device sector.
What matters most to him as a speaker: "Learning is a complex process. Especially in the health sciences, you're constantly facing new and evolving regulatory requirements. But training should also thrive on interaction and the shared experiences of participants and instructors. Together, we find the best solutions for every challenge."
