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Monitor CRO
About CRO
Full-service Turkish CRO offering clinical monitoring, data management, and regulatory submissions for pharmaceutical and medical device studies.
Technology & Expertise
Our Clinical Operations & Trial Management, Site & Clinical Monitoring, Data Management & Biostatistics capabilities are central to the work we deliver at Monitor CRO. Programs can draw on feasibility, project management, site coordination, and study close-out; investigator-site coordination supported by remote and on-site oversight; data standards, cleaning, analysis plans, tables, listings, and figures, with methods and resources selected for the required phase, geography, and data package.
Core Services
We provide tailored support in Clinical Operations & Trial Management, Site & Clinical Monitoring, Data Management & Biostatistics. Each Monitor CRO engagement can combine study start-up, cross-functional trial oversight, and operational delivery; site feasibility, activation, monitoring, issue management, and close-out; clinical database design, data review, statistical programming, and analysis, configured for the required study phase, markets, and internal sponsor resources.
Accreditations & Compliance
Our public materials reference ICH, GCP. At Monitor CRO, quality requirements are defined for the service, facility, jurisdiction, and study scope. We provide current certificates and site-specific documentation for review during vendor qualification.
