OUR SOLUTIONS

We offer comprehensive solutions while taking into account the challenges of cost effectiveness, time savings and increasing regulatory constraints.

Our expertise in various therapeutic areas and in-depth support at all stages of medical device lifecycle allows us to be the partner of choice to achieve your goals.

REGULATORY EXPERTISE
This stage ensures the safety and performance of a medical device is based on sufficient clinical evidence throughout its life on the market. Our team includes CER experts who have worked on complex devices. Read more

We have extensive expertise in this pivotal step, usually conducted to produce clinical data to support clinical performance and/or safety in the context of CE marking. Read more

This post-CE marking clinical follow-up consists of collecting real-life clinical data to confirm the medical device performance and safety claims. Rely on our dedicated team to successfully complete this step and maintain your device on the market. Read more

RWE  is a powerful tool to help manufacturers demonstrate the safety and performance of their devices. To be able to ingest, standardize, and connect the heterogeneous datasets collected is critical to creating insightful analytical results: this is a mission you can entrust to Eclevar. Read more

The commercialization of your medical devices is the fruit of numerous studies, R&D and in-depth analyses, confirming its safety and performance. Eclevar is the partner of choice to assist you in your CE marking process. Read more

Hospitals

Therapeutic areas

Eclevar operates in a wide range of medical fields and designs solutions adapted to the challenges of medical device manufacturers.

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THE ECLEVAR TEAM

We are is powered by the people who work in the organization, united around common values. Discover our global team of experts.

healthcare technology

OUR MISSION AND VALUES

We help our clients provide patients with safe and effective medical devices through tailored services.