Innova Trials | Reach Beyond | CRO Services in Latin America

Our commitment

We work hand in hand with our clients and partners to drive innovation in healthcare, with the goal of generating a positive impact and transforming the quality of life of people around the world.

Our commitment

We work hand in hand with our clients and partners to drive innovation in healthcare, with the goal of generating a positive impact and transforming the quality of life of people around the world.

Your CRO Expert For Latin America

Our Services

Feasibility and site selection.

Regulatory requirements to conduct the study.

Study set-up and startup phase.

Budget and contract negotiation.

Logistics and Importation process.

Vendor selection and management.

Project overview and monitoring.

Cutting-edge technology for clinical trial management (Alpha-CR)

View About Us

Feasibility and Site Selection

We have a pre-qualified sites network working with us in the different countries across Latam. These sites have gone through a rigorous feasibility process assessing patient availability, site capabilities and working procedures. We prioritize high-performing sites with proven track records to ensure fast recruitment, compliance, and study success.

Regulatory Requirements to Conduct The Study

We provide our clients with a clear overview of the regulatory requirements needed to initiate a clinical trial in each country. Our team ensures all necessary documents required in each step to obtain the study approval from the IRBs, ECs, MoH (Institutional Review Board, Ethics Committee, Ministry of Health).

Study Set-Up and Startup Phase

Efficient coordination of all startup activities to ensure a fast and compliant study launch. Our proactive approach minimizes delays and identifies potential obstacles to ensure a smooth study launch and avoid unnecessary and predictable hold-ups.

Logistics and Importation Process

We manage the end-to-end importation and logistics of clinical supplies, ensuring regulatory compliance and timely delivery to the depot. Our expertise helps navigating customs processes efficiently avoiding potential delays. A smooth importation process is key in any study success.

Vendor Selection and Management

We contribute in identifying the external vendors needed along the study and oversee them during the clinical trial to ensure high-quality performance, compliance with regulatory requirements and alignment to study timelines and objectives.

Project Overview and Monitoring

We provide ongoing coordination and oversight of study progress through on-site and/ or remote monitoring, risk assessment and performance tracking. Our team ensures adherence to protocol and local and international regulations, timelines and quality standards, keeping our clients informed at every stage.

Our partners