Clinical Development
Ensuring safety and measuring the effectiveness of our solutions
To continuously assess the safety and performance of its implants, Cousin has structured a clinical development activity in collaboration with expert centers, in compliance with the requirements of European Regulation (EU) 2017/745.
6
Ongoing clinical studies
72
Publications
The Cousin clinical team’s mission is to produce, analyze, and share data to continuously assess the safety and performance of our implants. It is involved throughout their life cycle, from development to long-term post-market clinical follow-up.
In close collaboration with investigator surgeons, we conduct studies prior to CE marking of our implants and as part of post-market clinical follow-up (PMCF).
These clinical studies are conducted in compliance with the requirements of European Regulation (EU) 2017/745 and are based on ISO 14155, the standard for good clinical practice for medical devices.
Our team also develops specific registries, with the collaboration of many surgeons in France, who continuously collect clinical data relating to the use of Cousin implants in routine practice.
Clinical Books
Cousin clinical books bring together all clinical data produced by our teams.
These resources are reserved for healthcare professionals and related professionals registered on our website.
Visceral Surgery /
Abdominal wall reinforcement:
hernias and incisional hernias
Spine Surgery /
Dynamic stabilization
Hernia Club / Clinical registry
Many surgeons contribute to the Hernia Club registry by entering clinical data relating to
the use of our implants.
Team
Mathilde COLLET
Clinical Manager
Margaux Silver
Clinical Research Associate
Contact us
Please feel free to contact us with any questions related to the clinical studies in which Cousin participates or any clinical study project.