We are a Contract Research Organization (CRO) specializing in Clinical Data Management, eCRF design and programming, biostatistics, and the implementation of Clinical Data Standards (CDISC CDASH and SDTM). Our services also include Quality Assurance and Outsourcing for Clinical Trials across Phases I–IV, as well as Epidemiological Studies, Real-World Evidence (RWE), and Outcomes Research.
We operate in Latin America and serve clients worldwide. We work together with Pharmaceutical and Biotechnology companies, and other Contract Research Organizations (CROs) in Clinical Data Management, standardization of clinical data and tabulation of gathered raw data to the CDISC-SDTM standard, which allows them to successfully complete Regulatory Submissions in Electronic Format to FDA and other Regulatory Agencies.