R&DP

We focus on Clinical Data Management, eCRF Design/Programming, CDISC-SDTM Data Tabulation projects, Clinical Data Standards (CDISC-CDASH / SDTM) & Biostatistics for Clinical Trials in Latin America and 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.