We offer a comprehensive range of expert services designed to advance cardiovascular research. Our solutions, from trial management to core laboratory analysis, ensure the highest standards of quality and reliability at every stage of your clinical research.
CERC provides exhaustive services and expert assistance in the whole cycle of clinical trials.
CERC regulatory know-how ensures that all regulatory requirements are fulfilled before patient enrolment in compliance with MDR, FDA, PMDA, GDPR and other applicable regulations.
CERC expertise includes ECG ECHO, CT-SCAN, MRI, angiography, IVUS, and OCT analysis.
CERC offers expert guidance and a comprehensive array of services to industry partners, ensuring the development of top-tier clinical strategies across the entire product life cycle.
CERC provides expert guidance for IIT optimization and logistics and can manage the full project from acting as a Sponsor through trial execution until publication.
CERC is a leading Contract Research Organization based in Massy, France, specializing in cardiovascular clinical research.
Founded in 2008, by physicians with extensive experience in cardiology, CERC builds strong scientific, premium, innovative research solutions.
Our multidisciplinary teams collaborate closely with industry partners and academic investigators to advance new technologies, techniques, and treatments for better patients care.
The first patient in Latvia was enrolled on October 1 at Paula Stradiņa Klīniskā universitātes slimnīca in Riga, under the leadership of Principal Investigator Prof. Andrejs Erglis. Congratulations to Prof. Ērglis and the entire study team for reaching this important milestone. Sponsored by CERIC...
Get in touch with our team for more information or support.
Adresse
7 rue du Théâtre
91300 Massy, France
We offer a comprehensive range of expert services designed to advance cardiovascular research. Our solutions, from trial management to core laboratory analysis, ensure the highest standards of quality and reliability at every stage of your clinical research.
