CONTRACT RESEARCH
ORGANIZATION
Dedicated to help companies and
health care professionals with their clinical research in Europe.
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Full-service CRO
Supporting every step of your clinical research. We offer high-quality services for regulatory consultancy and clinical study management, as well as data management, biostatistics and medical writing.
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Specialized in complete life cycle support for medical devices
We deliver valuable clinical data for medical devices to meet the medical needs for the patient and to continuously monitor the quality and safety of the device during the device lifecycle.
With a personal approach
Our dedicated monitors are a supportive extension of the study team. We are actively involved, enforcing our relationships and thereby reaching your project goals and timelines.
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CONNECTED GLOBALLY
Expanding borders, local feel
Archer Research is located in the heart of Europe, covering studies across Europe and The UK, with a partner in the United States.
We help customers worldwide navigate the MDR clinical evidence requirements, while ensuring compliance with European legislations.
In addition, our US partner provides expert support for FDA approvals, facilitating US market access.
We have built a strong network that serves clients worldwide, allowing us to bring international expertise to every project, whilst maintaining a personalized local approach.
OUR PARTNERS
ABOUT US
Introducing: Our dynamic team of experienced research professionals eager to advise you and drive your project with the highest quality. Let us do what we do best. Let us run your project. We are crazy about clinical research!
Nice to meet you!
Karen Gabriels
PhD, Clinical Research Manager
MDR expert helping you find your way through the regulatory web.
Mieke Tempels
MSc, Clinical Operations &
Quality Manager
Clinical operations expert, supporting the team in delivering all projects with the highest quality.
Dorien Haesen
PhD, Clinical Project Manager
Project management expert supporting the sponsor and leading the project team in ensuring timely and compliant study execution.
Stephanie De Munter
PhD, Clinical Project Manager
Project management expert supporting the sponsor and leading the project team in ensuring timely and compliant study execution.
Liesbeth Coteur
MSc, Clinical Project Manager
Project management expert supporting the sponsor and leading the project team in ensuring timely and compliant study execution.
Frea Coun
Clinical Research Associate
Data expert with the highest dedication to monitoring clinical studies and supporting the site staff as an extension of the study team.
Tim Enis
Clinical Research Associate
Data expert with the highest dedication to monitoring clinical studies and supporting the site staff as an extension of the study team.
Lauren Swinnen
PhD, Clinical Research Associate
Data expert with the highest dedication to monitoring clinical studies and supporting the site staff as an extension of the study team.
Els Coenen
MSc, Clinical Research Associate
Data expert with the highest dedication to monitoring clinical studies and supporting the site staff as an extension of the study team.
Wouter Wilms
Clinical Trial Assistant
Supporting the team with day-to-day administrative activities, keeping things running smoothly and efficiently behind the scenes.
Eline Bruyninx
Management Assistant
Dynamic organisation talent, making our days super efficient and bright.
OUR
COLLABORATIONS
Need support with your clinical research?
Let our research professionals assist you.
CONTACT US
Agoralaan A bis (BioVille) - 3590 Diepenbeek - Belgium
REGULATORY EXCELLENCE
YOU CAN TRUST
At Archer, quality, compliance, and data security are at the core of everything we do.
We are committed to upholding the highest industry standards to ensure the integrity, safety, and efficiency of clinical research.
We work conform internationally recognized standards and regulations, that reflect our dedication to excellence.