Javier Castillo

I have worked in the Medical Device industry for 14 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 a successful closure of series B in different companies, with funding rounds of 35 and 54 M€.