I have worked in the Medical Device industry for 10 years, with relevant experience in the Quality and Regualtory and Risk Management for several devices from Class I to Class III, in the EU market and US market. I have experience with the regulatory clearance process with the FDA and CE marking with several Notified Bodies in the EU. I obtained regulatory clearance for clinical trials in the EU and the US. I have participated in a due diligence process that led to the closure of a funding round of 34.4 M€.
I heard about you from one of my network contacts from a Venture Capital