Eclevar Medtech

Eclevar Medtech is a specialized Contract Research Organization (CRO) that provides end-to-end clinical and regulatory solutions for the medical device and in-vitro diagnostic (IVD) industries. The company offers a wide range of services, including clinical trial design and management, regulatory strategy, and post-market clinical follow-up (PMCF) studies. Eclevar is particularly noted for its expertise in helping manufacturers comply with the European Union's Medical Device Regulation (MDR) and In-Vitro Diagnostic Regulation (IVDR). By integrating digital technologies into clinical data collection, the firm aims to streamline the path to market for innovative medical technologies. Their global reach supports clients in navigating diverse regulatory landscapes across Europe and North America.