Archer Research is a full-service Contract Research Organization (CRO) specialized in clinical research with Medical Devices, covering studies all over Europe and The UK.

For our clients, we are a partner from the very beginning along the full lifecycle of their clinical development. Whether you are an early-stage start-up or a large organization or an investigator, we can help you achieve your strategic goals through sound clinical and regulatory planning and execution.
We are experts in setting up and managing pre-CE as well as post-market clinical follow-up studies from A to Z.
- Regulatory and clinical strategy, clinical development planning
- Clinical evidence, literature review, gap assessment of available data
- Medical writing from clinical evaluation (CEP/CER) to clinical study protocol/CIP, ICF to Clinical Study Report and manuscript.
- Investigational site selection, Ethics & Regulatory submissions, contract set-up, payment management, study set-up & planning.
- Case report form (CRF) design, electronic data capture (EDC) programming, biostatistical analysis and sample size calculation, as well as Data Management.
- Project Management and Study monitoring activities (risk-based, remote and/or on-site).
- Expert in the Medical Device Regulation (EU MDR) and the requirements for medical device companies in obtaining valuable clinical data compliant with ISO14155 and GDPR.

Why do we stand out?
- Full-service CRO
- Specialized in Medical Devices
- Personal approach
- Covering Europe & The UK

Welcome to come in for a coffee in our offices in Diepenbeek, Belgium, or to meet virtually if you are interested to know more about Archer! Only an email away via info@archerresearch.eu.

Feel free to follow our LinkedIn page and visit our website to stay up to date about our services, our achievements and the amazing people behind Archer.
http://archerresearch.eu

Archer Research

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