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.
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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Board of Directors
Qserve Group was founded in 1998 by Willibrord Driessen with a small team of regulatory experts and has since grown into a globally recognized player in the medical device industry, with offices in Europe, the United States, and China.
Since 2014, three new shareholders strengthened the Board of Directors, united by Willibrord's global vision. In 2026, Inette Nieveen-van de Laar became the newest member of the Board, bringing over a decade of expertise and leadership within Qserve to that role.
The Board, now comprising Jan van Lochem, Martin de Bruin, Gert Bos, and Inette Nieveen-van de Laar, is committed to growing Qserve Group and Qserve CRO into a leading global medical device consulting group. Qserve specializes in regulatory and clinical affairs, Regulatory Intelligence, Quality Assurance, Clinical Research, and Training, supporting manufacturers worldwide in gaining registration, approval, and market access.
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Over the past 28 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.
We have 7 offices worldwide
Get in touch to learn more
Meet our team of professionals
Jan van Lochem, MSc, MBA
Chief Executive Officer (CEO)
Partner
Martin de Bruin, MSc
Chief Commercial Officer (CCO)
Partner
Gert Bos, PhD
Chief Scientific Officer (CSO)
Partner
Inette Nieveen, MSc
Chief Operating Officer (COO)
Principal Consultant
Bianca Lutters, PhD
Director of Knowledge Management
Regulatory and Clinical Expert
Principal Consultant
Jorn van Binsbergen, MSc
Senior Consultant
Regulatory and Clinical Expert
Claire Borde, PhD
Sr. Clinical Project Manager
Maria Cámara Torres, PhD
Consultant
Clinical Expert
Minghua Chen
Business Development Manager Asia-Pacific
VP Regulatory Compliance
Mindy McCann
Country Manager US
Principal Consultant
Patrícia da Silva Perez, PhD
Team Manager Clinical Writing
Biocompatibility Expert
Senior Consultant
Coenraad Davidsdochter, MSc
Team Manager Regulatory & Quality
Software Expert
Senior Consultant
Nienke Flipsen-Maassen, MSc
Senior Clinical Data Manager
Nicolas Garrett
IVD Regulatory Expert
Consultant
Adriana Gavrilciuc, MSc
Regulatory Affairs Expert
Senior Consultant
Olena Hoi, MSc
Regulatory and Quality Affairs Expert
Senior Consultant
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Stephanie (Xing) Huang
Principal Consultant
NMPA Expert
Country Manager China
Floor Janssen
Clinical Writer
Tim Joiner, MSc
Senior Consultant
Regulatory and Quality Expert
Kevin Kenney
Senior Consultant
Design and Safety Compliance Expert
Jelena Kresoja, MSc
Consultant
Regulatory and Clinical Expert
Jiuru Li
Clinical Writer
Bingshuo Li, PhD
Senior Consultant
Regulatory and Software Expert
AI Lead
Dulce Aguilar, PhD
Clinical Writer
Dr. Cornelia Luban, PhD
Principal Consultant
Regulatory Affairs Expert
Wouter Mattheussens, MSc
Clinical Project Manager
Keith Morel, PhD
Principal Consultant
VP Regulatory Compliance
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Amé Huige
Marketing Specialist
Manager Training Marketing & Development
François Naye, PhD
Senior Consultant
Training Expert
Software Expert
Quality Expert
Regulatory Expert
Robert Paassen, MSc
Team Manager Regulatory
Quality Expert
Senior Consultant
Start-up Lead
Swaroop Rani Kesevan Nair
Consultant
Regulatory Affairs Expert
Cécile Rosset
Senior Consultant
Regulatory Affairs Expert
Dennis Sarwin, MSc
Team Manager Global Registrations & Consultant
René Schings
Quality and Auditing Expert
Principal Consultant
Kristiane Schmidt, PhD
Principal Consultant
IVD Lead
Agnieszka Schreiber, BEng
Senior Consultant
Regulatory and EUDAMED Expert
Jennifer Simon, MSc
Consultant
Regulatory Expert
Melissa Smits
Regulatory Affairs Associate
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Daphne Smit-van den Hof
Sr. Clinical Project Manager
Joshua Spencer
Global Registrations Specialist
Stephanie Valk, MSc
Director Business Control
Regulatory and Quality Expert
Principal Consultant
Jeff Habecker
Business Development Manager North America
Ricardo Azuero
Business Development Manager EU
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Celien van Lochem
Business Development Manager CRO
Manager Training Operations
Iris Verboven
Business operations Manager Clinical
Pim Kolsteeg
Director HRM & Finance
Yaël Salakory
HR Generalist
Sruthy Jayakumar Nair
Application Specialist
Cindy Soumage
Project Management Officer
Jose Castilla Martin
Marketing Manager
Thomas Peters
Marketing & Communication Specialist
Patrick Bouwman
Financial Controller
Stella Osuji
Assistant Controller
Stefan Worm
Assistant Controller
Colleen Rimel
Assistant Controller
Gabriela Grozdanova Andonova
Legal Counsel
Global Registrations Specialist
Mendy Belt
Global Registrations Specialist
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Malou van Loon
Clinical Research Associate
Bente Horsting
Junior Marketing Specialist
Ryan Hartman
Junior Sales & Project Management Officer
Oliver Schaer
Business Development Manager DACH
Poonam Babu Ram
HR Officer
Sofia Honorio-Grand
Clinical Project Manager
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Mike Szymonik
Senior Consultant
Regulatory Expert IVD and MD
Sanne Hartemink-Schouten
Clinical Trial Assistant
Jose Cabrera
Principal Consultant
US Market Expert