Medex CRO
Full-service contract research organisation, since 2022
Medex CRO runs clinical studies end to end for sponsors in Türkiye: regulatory and ethics submissions, site start-up, monitoring, pharmacovigilance, data management and biostatistics, from Phase I–IV to medical devices. It grew out of the SMO network, so sites and sponsors share one team.
What it does
- Regulatory affairs and ethics committee submissions (TİTCK)
- Clinical operations and monitoring
- Data management, biostatistics and medical writing
- Pharmacovigilance
- Medical device evidence: clinical investigations, CER, PMCF