SUPPORT & EXPERTISE
about us
ECLA (Estudios Clínicos Latinoamérica) is an Contract Research Organization (CRO) devoted to provide support and expertise for the conduct of clinical trials in Latin American since 1987.
We provide academically oriented planning, coordination and management of international multicenter clinical trials. We facilitate start-up and operation of clinical trials with the goal of providing top-notch clinical research services.
OUR SERVICES
Our expertise in clinical trials ensures the highest quality services, rigorous processes, and accurate outcomes to support innovation in health care and pharmaceutical development.
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Academic Leadership
• Overall trial guidance
• Expert scientific support for clinical research projects
• Participation in scientific organizations and Steering Committees -
Regulatory Management
• Competent regulatory authorities end-to-end submissions (Ministry of Health and local Ethics Committees)
• Serious Adverse Events/Adverse Events management and safety reporting -
Project and Site Management
• Investigators and site identification
• Feasibility assessment
• Site selection, training and activation
• Continuous support to site staff -
Patient Recruitment Strategies
• Motivational Meetings
• Strong and long-standing relationship with Investigators and high-quality sites -
Monitoring
• Onsite Monitoring
• Remote Monitoring
• Risk-based monitoring -
Quality Assurance
• Internal and external audits
• Inspection readiness
• SOPs development and compliance training -
Data Management
• CRFs and databases design and management
• Data entry, data validation and query generation
• IWRS -
Pharmacy
• Management of drug and study material (accountability, reconciliation and destruction)
• Coordination of local drug storage and distribution -
Logistics and Management
• Importation and distribution of Investigational Product
• Coordination of temperature-controlled shipments
• Coordination of biological samples collection, storage and exportation -
Finance and Legal Department
• Management of trial insurance
• Negotiations and execution of Site Agreements
• Site payments -
Medical Writing
-Protocol development
• Regulatory documentation
• Scientific writing
• Bilingual support
CLINICAL RESEARCH
We have conducted numerous clinical trials on different therapeutic areas.
DRIVING CLINICAL RESEARCH WITH EXCELLENCE AND INTEGRITY
we cover all medical specialties
OUR LEAD TEAM
Our vision is founded on a legacy of scientific excellence and strengthened by a new generation of leadership. Guided by the expertise of our founder and inspired by forward-looking perspectives, we are committed to advancing clinical research with rigor, integrity, and global impact. Together, we transform innovation into evidence and evidence into better health outcomes worldwide
