About us

Global reach, practical advice, experienced team!

About us

Your MedTech Partner for Regulatory, Quality Affairs and Clinical Trials

Our benchmark is the unique combination of a global reach, high level expertise and staff with field experience. All consultants had former positions at medical device manufacturers, European Notified Bodies, US FDA or Chinese CFDA.

The Qserve Team

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Qserve Mission 

Our mission is to help improve patient safety and health through supporting the advancement of biomedical technology. We assist medical device and in-vitro diagnostics manufacturers worldwide with market access, medical device approvals, clinical trials and achieving and maintaining regulatory compliance. We strive to do this with a practical approach balancing business needs and regulatory compliance. We are passionately working for our customers on regulatory, quality and clinical challenges and see it as our responsibility to create a diverse global team of professionals who share the same passion for medical device technology, a high standard of quality, competence and customer service, and enjoy the fun of working on this together every day. Our people make our firm.

History and Management Team

Qserve Group is founded in 1998 by Willibrord Driessen and started with a small group of regulatory experts. Since 2014, three new shareholders joined the Board of Directors with the strong aim to continue in line with Willibrord's global vision. Now, Qserve is a global player, well known among medical device manufacturers, with offices in Europe, US, and China.

The current Board of Qserve group consists Jan van Lochem, Martin de Bruin and Gert Bos. They will continue to expand Qserve Group as a leading global medical device consulting group in Regulatory Compliance, Clinical Trials, Quality Assurance, and training to enable registration, approval and market access of medical devices in global markets.

        Jan van Lochem, Martin de Bruin and Gert Bos

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