Archer Research
Information
ARCHER RESEARCH is a full-service Contract Research Organization specialized in clinical evaluations and clinical investigations with MEDICAL DEVICES, located in the heart of Europe with a fast connection between Belgium, France, The Netherlands, The UK and Germany, and covering studies all over EUROPE.
For our clients, we are a partner from the very beginning along the full lifecycle of their device clinical development. Whether you are an early-stage start-up, 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 clinical evaluations and setting up and managing pre- and post-market medical device clinical studies from A to Z.
- Clinical evaluation plan and report (CEP & CER) writing
- Ethics Committee and Regulatory Authority submission and approval, contract set-up, payment management, study planning and investigational site selection.
- Case report form (CRF) design, electronic data capture (EDC) programming, biostatistical analysis and sample size calculation, as well as clinical study Project Management.
- Study monitoring activities (risk-based, remote and/or on-site), as well as medical writing from clinical evaluation to clinical study protocol/CIP, Informed Consent Form to Clinical Study Report and manuscript.
- We are expert in the Medical Device Regulation (MDR) and the requirements for medical device companies in obtaining valuable clinical data.
Why do we stand out?
- Full-service CRO
- Specialized in Medical Devices
- Personal approach
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.
