Our Management Team

President & CEO of Qserve Consultancy and the Qserve Group, Willibrord Driessen has held a number of key management positions in the Medical Device Industry. He brings more than 25 years of senior management skills to the Qserve Group in the areas of Quality Management Systems and Regulatory Affairs. Willibrord is a qualified Lead Auditor holding Notified Body certification and CMDCAS certification

Willibrord’s particular fields of expertise are in the implementation and management of quality management systems ISO 13485:2003, CMDCAS, ISO 9001 and auditing. Willibrord has extensive knowledge of international regulatory affairs, and has specialist knowledge of CE Marking. He is also an experienced coach of senior managers and is a qualified trainer in all aspects of quality management systems, auditing, and regulatory affairs.

Cell: +31 6 5375 0455
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Peter Ruys is an expert consultant in International Medical Device regulations and served as Certification Manager for medical devices with the Notified Body KEMA Quality.

Peter earned his degree in physics while attending the University of Utrecht. In 1975, he was appointed as a clinical physicist for Radiation Therapy and Nuclear Medicine at the Free University of Amsterdam. He was elected to the board of directors of the medical faculty two years later in 1979. Five years later, he was appointed as manager of the Department of Biomedical Engineering and Clinical Physics at the University hospital. In 1992, KEMA invited him to initiate Notified Body activities in the field of medical devices. Peter has served as vice-chairman of the Notified Body that meets in Brussels and has lectured at several seminars in Asia, Europe and the USA.

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Jeannette van Loon is an expert consultant in Medical Device Regulation, Standardization and Safety Evaluation.

Earlier in her career, Jeannette worked as Chief Operating Officer at a test and research laboratory specializing in the biocompatibility and biological safety testing of medical devices. She has served as a senior standardization consultant at the Dutch Standardization Institute (NEN) and Sector Healthcare. She also has worked as an independent advisor and coordinator of National, European and International standardization processes pertaining to the fields of medical devices, tissue engineered products and human tissues. Holding a PhD degree in biomaterials, Jeannette wrote her doctoral thesis about "biocompatibility testing of degradable polymers."

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Bill brings to Qserve over 23 years of medical industry experience, including 13 years spent as a senior manager.

Bill’s wide range of expertise includes: Strategic regulatory planning, Global quality system development, CE Marking, New technology assessment, Business development and Medicare reimbursement. Having served at various times as C.F.O, C.O.O, V.P. Operations, General Manager Sales and Marketing, and as a Director and Corporate Secretary, he has acquired a unique understanding of both the needs and the contributions of the various departments and disciplines within an organization and how they interact at all levels to achieve a common corporate goal.

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