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CTI Clinical Trial and Consulting Services
About CRO
Full-service clinical trial management organization providing Phase I-IV clinical research, regulatory, and consulting services.
Technology & Expertise
CTI combines global clinical operations with therapeutic and regulatory expertise across the development lifecycle. Its delivery model integrates project leadership, site and patient strategy, clinical monitoring, biometrics, safety, medical writing, laboratory support, and consulting. The organization emphasizes complex and critically ill patient populations and applies cross-functional planning to connect protocol design, operational execution, data review, and regulatory objectives across participating countries.
Core Services
Core services include development strategy, protocol and study planning, feasibility, site identification and activation, project management, clinical monitoring, patient-recruitment support, data management, biostatistics, statistical programming, medical monitoring, pharmacovigilance, regulatory affairs, medical writing, quality assurance, and clinical-study reporting. CTI also provides consulting and specialized research support from early development through late-phase studies and commercialization planning, using full-service or functional delivery models.
Accreditations & Compliance
CTI supports regulated clinical programs through SOP-based quality management, qualified personnel, documented oversight, audit readiness, and inspection support. Studies are managed according to the applicable ICH Good Clinical Practice principles, protocol requirements, ethics approvals, safety-reporting obligations, data-protection rules, and national regulations. Quality controls may include vendor qualification, investigator-site and process audits, issue escalation, CAPA management, and training. Country-specific licenses, laboratory credentials, and study accreditations should be confirmed during qualification.
