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Intrials
About CRO
Spanish CRO providing clinical development, regulatory consulting, and data management services with expertise in oncology and rare diseases.
Technology & Expertise
Our Clinical Operations & Trial Management, Regulatory Affairs & Submissions, Data Management & Biostatistics capabilities are central to the work we deliver at Intrials. Programs can draw on feasibility, project management, site coordination, and study close-out; planning and delivery of regulatory documents across development milestones; 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, Regulatory Affairs & Submissions, Data Management & Biostatistics. Each Intrials engagement can combine study start-up, cross-functional trial oversight, and operational delivery; regulatory strategy, dossier development, submission management, and authority support; 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 Intrials, 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.
