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Gert Bos
Executive Director & Partner at Qserve Group, The Netherlands

Profile

Gert is an expert in European regulations based on 15 years hands-on working in the field, as auditor, product reviewer, regulatory specialist, and Head of notified body. 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 with a large range of devices mostly in the non-active device area. For his contributions to the regulatory profession over the last 15 years he has been awarded as Fellow of RAPS.

Agenda Sessions

  • Moderated by GERT BOS Executive Director & Partner at Qserve Group, The Netherlands

    10:30
  • Streamlining the Processes Between Clinical Evaluation and Post Market Surveillance to Better Leverage Data

    13:20

Speakers at this event