Medical Device Project B.V.
As Principal Consultant at Medical Device Project B.V. in the Netherlands, Robert van Boxtel is assisting medical device manufacturers with their QMS, technical files and regulatory submissions, both in the EU and USA.
In addition to that, he is hired by the Dutch Standards Institute (Royal NEN), as SME for teaching on ISO 13485 and MDD/MDR. Furthermore, he participates in TC210 discussions on risk management, ISO 13485 and PMS.
Before joining Medical Device Project B.V., he worked at KEMA Quality Notified Body (now Dekra) and in the medical device industry. As a result he has 25 years of experience in the medical device industry.
Robert is a member of the board of the RAPS Netherlands Chapter .
Tuesday, October 27, 2020
16:15 – 17:45 CET