PARTNER OF YOUR
MEDICAL DEVICES LIFECYCLE​

ECLEVAR MEDTECH is a global CRO, headquartered in Paris. We support medical device and IVD manufacturer in the MDR and IVDR transition. Our team works as an extension team of medical affairs and regulatory affairs sponsor.
We offer customized service, personalized to the need of our clients. Whether you are looking for full service CRO or staffing clinical or regulatory experts, our management team with more than 20 years experience will drive you to the effective solution

VALUES

An agile CRO for complex clinical studies

MISSION

Make clinical trials affordable to the Medtech industry

VISION

Cost effectiveness, time savings and management of regulatory constraints.

THE ECLEVAR POWERHOUSE

A SKILLED TEAM OF EXPERTS

Eclevar is made up of passionate and multicultural people with strong skills and experience in their field of expertise.

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A scientific board

Composed of prominent KOLs, its role is to supervise the entire process and guarantee clinical and scientific validity of our approach.

REGULATORY EXPERTISE

Our teams master regulatory topics, thus helping our clients to face the challenges of accessing international markets safely and efficiently.

“Regulatory evolutions differ from one region to another: they have their own rules and requirements for medical devices. It is crucial to partner with a CRO that understands and handles these challenges.”

Chems Hachani
CHEMS HACHANI
CEO, Eclevar