Partner & Chief Scientific Officer (CSO)
QServe Group
Baarn, Gelderland, Netherlands
Gert is an expert in European regulations based on more than 25 years hands-on working in the field, as auditor, product reviewer, regulatory specialist, Head of notified body and strategic, regulatory and business consultant.
He has been leading the Notified Bodies in Brussels for many years, and has strongly supported the regulatory debate with the EU Commission, EU Parliament and the EU Council of Ministers.
He combines strong experience in quality, compliance and regulations with a pragmatic, result driven approach at both operational and strategic level.
From his PhD in Biomaterial Sciences, and PostDocs in controlled release of drugs and gene therapy, he has dealt as technical reviewer and consultant with a large range of devices mostly in the non-active device area.
For his contributions to the regulatory profession he has been awarded as Fellow of RAPS. He is a recipient of the RAPS founder's award.
Wednesday, May 6, 2026
08:30 - 09:30 WEST
Meet the Authors: Software as a Medical Device (Second Edition)
Wednesday, May 6, 2026
09:45 - 10:45 WEST
Simplification and Centralization
Wednesday, May 6, 2026
10:45 - 11:45 WEST
Wednesday, May 6, 2026
13:30 - 13:55 WEST
Clinical Evidence as the Cornerstone of MDR Compliance: Lessons, Challenges, and the Road Ahead
Wednesday, May 6, 2026
14:30 - 15:30 WEST
Solutions Circle 1: Compliance Amidst Uncertainties for Medical Devices
Thursday, May 7, 2026
09:40 - 10:10 WEST
Thursday, May 7, 2026
14:30 - 15:30 WEST
Solutions Circle 2: Compliance Amidst Uncertainties for Medical Devices
Friday, May 8, 2026
10:10 - 10:40 WEST
Friday, May 8, 2026
11:15 - 12:15 WEST