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Regulation, Clinical and Software for Medical Devices


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November 5 - 7, 2024
The Royal Sonesta Minneapolis DowntownMinneapolis, Minnesota

Gert Bos
Executive Director & Partner at Qserve Group


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.

Gert is chairman of the board of RAPS and member of the RAPS EU board.

Agenda Sessions

  • Inviting Innovation: Encouraging Innovative Devices back to Market

  • A Transatlantic Update: Regulating Medical Devices in Europe

  • Ask the Experts: Medical Devices