About · Latin America CRO
Latin America CRO
MediTrans Clinical S.A.S. — Clinical CRO based in Colombia.
Local clinical execution connected to MediTrans clinical and regulatory documentation capability.
Local delivery. Global quality.
MediTrans Clinical S.A.S. is the MediTrans Group’s Latin America CRO affiliate.
Based in Colombia, it supports regulatory, feasibility, monitoring, and data operations for clinical studies, helping strengthen site and investigator access—while connecting to MediTrans Korea’s medical writing and clinical/regulatory documentation capability for smoother Asia–LATAM programs.
Why Latin America
From patient access and multinational operating efficiency to quality and market potential, we support sponsors who choose Latin America for multi-regional clinical development.
Patient access
High urbanization and concentrated metropolitan populations can support stronger enrollment, with disease prevalence patterns comparable to major markets.
Multinational operating efficiency
Spanish- and Portuguese-centered regional operations help streamline multinational clinical communication and document readiness.
Quality & compliance
We focus on local regulations, medical practice, and GCP-aligned monitoring to protect trial compliance and data integrity.
Market potential
Participation in multi-regional trials can support later registration and access strategies—so regional planning starts early.
Why Colombia
Colombia is recognized as a growing clinical research hub, combining trained investigators, competitive operating costs, and access to diverse patient populations.
- Practical knowledge of local regulation, ethics committees, and site relationships
- Skilled clinical research talent with multilingual communication capability
- Efficient infrastructure and operating cost structure versus US/EU settings
- A growing CRO market sought by global sponsors, MedTech, and pharma
- Links to local university and hospital research networks (e.g., UNAL)
CRO services
Operational CRO support across the study lifecycle, complemented by MediTrans medical writing and clinical/regulatory documentation expertise.
Regulatory Affairs
Support for local submissions, ethics, and regulatory requirements
Protocol Development
Protocol development support aligned to therapeutic area and phase
Feasibility
Country, site, and patient feasibility assessment before launch
Clinical Monitoring
Site monitoring for protocol adherence and data quality
Data Management & Biostatistics
Clinical data management with biostatistics collaboration
Pharmacovigilance
Support for safety information collection and reporting workflows
eCRF
Electronic case report form design and operational support
Staff Support
Clinical research staffing and study-stage field support
One group bridging Asia and LATAM
Local CRO execution alone is not enough—and documentation alone does not move sites.
MediTrans Clinical and MediTrans connect both sides inside one group.
Local CRO execution
Feasibility, monitoring, regulatory, and data operations in Colombia and Latin America.
Clinical & regulatory documentation
Medical writing, clinical/regulatory documentation, and audit/inspection communication for global-ready submissions.
One-team handoff
Sponsors, CROs, and sites stay aligned on terminology, timelines, and quality standards.
Talk with us about Latin America CRO projects
Need Colombia CRO operations, multinational feasibility, or Asia–LATAM documentation support? Contact us.
Partnership / project inquiry About MediTrans
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