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CONTRACT RESEARCH
ORGANIZATION

Dedicated to help companies and

health care professionals with their clinical research in Europe.

Your personal partner to future proof 
your clinical evidence

We support you with the extensive and complex MDR clinical evidence requirements and challenges.

Our Services
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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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We match our services, expertise, budget & timelines to your specific clinical needs

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

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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!

About Us
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Karen Gabriels

PhD, Clinical Research Manager

MDR expert helping you find your way through the regulatory web.

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Mieke Tempels

MSc, Clinical Operations &
Quality Manager

Clinical operations expert, supporting the team in delivering all projects with the highest quality.

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Dorien Haesen

PhD, Clinical Research Professional

Project management expert with the highest dedication to support the site staff as an extension of the study team.

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Stephanie De Munter

PhD, Clinical Research Professional

Project management expert with the highest dedication to supporting the site staff as an extension of the study team.

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Frea Coun

Clinical Research Associate

Data expert with the highest dedication to supporting the site staff as an extension of the study team.

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Tim Enis

Clinical Research Associate

Data expert with the highest dedication to supporting the site staff as an extension of the study team.

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Lauren Swinnen
PhD, Clinical Research Associate

Data expert with the highest dedication to supporting the site staff as an extension of the study team.

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Els Coenen

MSc, Clinical Trial Assistant

Administrative wonder woman providing the best support for your project.

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Eline Bruyninx

Management Assistant

Dynamic organisation talent, making our days super efficient and bright.

"Partnering with Archer Research has been invaluable for advancing our clinical studies. Their responsiveness and expertise in the European market have streamlined every step, ensuring quality and compliance. Archer truly feels like an extension of our team, sharing our dedication to the research, patient well-being, and trusted partnerships with sites."

—  Timothy C. Cook, Ph.D.

President, CEO and Co-Founder Uromedica, Inc.

WHAT PEOPLE SAY

OUR 
COLLABORATIONS

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Need support with your clinical research?
Let our research professionals assist you.

CONTACT US

Agoralaan A bis (BioVille) - 3590 Diepenbeek - Belgium

Contact us

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.

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