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Cromos Pharma
About CRO
Mid-size CRO specializing in clinical trial management across Eastern Europe, Latin America, and other emerging regions for cost-effective trials.
Technology & Expertise
Our Clinical Operations & Trial Management, Site & Clinical Monitoring, Data Management & Biostatistics capabilities are central to the work we deliver at Cromos Pharma. 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 Cromos Pharma 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
At Cromos Pharma, 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.
