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About us
About Qserve Group

Qserve Group was founded in 1998 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 the global vision.

Mission and vision

Our mission is to help improve patient safety and health by 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 as your partner 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.

 

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Therapeutic Speciali

Our Therapeutic Specialties

We are widely recognized for our"practical" mindset—many of our consultants come from the MedTech industry, often having worked in regulatory, quality, clinical, or R&D roles or having been employed by notified bodies. This makes their advice practical, implementation-ready, and grounded in operational reality, not just theoretical knowledge. 

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Leadership

The board of Qserve Group

Qserve Group was founded in 1998 by Willibrord Driessen with a small team of regulatory experts. Since 2014, three new shareholders joined the Board of Directors, sharing Willibrord's global vision. Today, Qserve is a well-known global player in the medical device industry, with offices in Europe, the United States, and China, serving manufacturers worldwide.

The Board of Qserve Group includes Jan van Lochem, Martin de Bruin, and Gert Bos. They are committed to expanding Qserve Group and Qserve CRO into a top global medical device consulting group. We specialize in regulatory and clinical affairs, Regulatory Intelligence, Quality Assurance, Clinical Research and Training to help medical devices and diagnostics gain registration, approval, and market access worldwide.

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Qserve's historical growth

Over the past 27 years, Qserve has developed into a global company where the team combines their regulatory knowledge and experience in the medical device and in vitro diagnostic industry, sharing more than 500 years' worth of combined expertise in the medical field. 

The historical development shows Qserve makes you your global partner for Regulatory Compliance all over the world. 

 

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Our offices

We have 7 offices worldwide

Get in touch to learn more

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Meet our team of professionals

Jan van Lochem, MSc, MBA

CEO

Partner

Martin de Bruin, MSc

CCO

Partner

Gert Bos, PhD

CSO

Partner

Mindy McCann

Country Manager

VP US Operations

Amé Huige

Marketing Specialist

Manager Training Marketing & Development

Dulce Aguilar, PhD

Clinical Writer

Alexandra Beer, PhD

Quality Assurance and Auditing Expert

Jorn van Binsbergen, MSc

Clinical Writer

Claire Borde, PhD

Medical Writer

Renaud Brendel

Country Manager

Senior Consultant

Maria Cámara Torres, PhD

Medical Writer

Minghua Chen

Training Expert

MDR Expert

Patrícia da Silva Perez, PhD

Team Manager Medical Writing

Senior Consultant

Coenraad Davidsdochter, MSc

Team Manager Electrical Safety and Software/AI

Nienke Flipsen-Maassen, MSc

Data Manager

Nicolas Garrett

IVD Regulatory Affairs Expert

Adriana Gavrilciuc, MSc

Regulatory Affairs Expert

Olena Hoi, MSc

Quality and Regulatory Expert

Stephanie (Xing) Huang

Country Manager

Principal Consultant

NMPA Expert

Clinical Study Expert

Jasmin Hunter

Clinical and Regulatory Affairs Expert

Floor Janssen

Medical Writer

Tim Joiner, MSc

Quality and Auditing Expert

Kevin Kenney

Electromechanical Design and Safety Compliance Expert

Jelena Kresoja, MSc

Clinical Writer

Jiuru Li

Medical Writer

Bingshuo Li, PhD

Active Medical Devices Expert

Dr. Cornelia Luban, PhD

Regulatory Affairs Expert

Bianca Lutters, PhD

Head of Clinical Operations

Wouter Mattheussens, MSc

Clinical Project Manager

Mindy McCann, MSc

VP US Operations

Principal Consultant

Keith Morel, PhD

VP US Regulatory Compliance

Principal Consultant

Henk-Willem Mutsaers, MSc

Principal Consultant

Quality Assurance and Auditing Expert

François Naye, PhD

Senior Consultant

Training Expert

Software Expert

Quality Expert

Inette Nieveen, MSc

Head of Medical Devices

Robert Paassen, MSc

Regulatory Affairs Expert

Quality Expert

Swaroop Rani Kesevan Nair

Consultant

Cécile Rosset

Senior Consultant

Dennis Sarwin, MSc
René Schings

Quality and Auditing Expert

Principal Consultant

Training Expert

Kristiane Schmidt, PhD

Senior Consultant