Biostatistics & Programming

Overview

UBC provides comprehensive statistical services for all phases of clinical development and offers exceptional guidance with a critical eye on all emerging issues. Our biostatistics team offers unsurpassed skill and experience in designing protocols, developing and implementing statistical methodologies, and supporting regulatory submissions. UBC coordinates biostatistics, data management, SAS programming and medical writing to support clinical development from Phase I through Phase IV.

UBC biostatisticians and programmers offer unparalleled scientific expertise and operational skill. Our knowledge and experience is based on decades of participating on integrated drug development teams, hundreds of consulting assignments, participation on data monitoring committees, and direct interactions with local and international regulatory bodies, including the FDA, EMEA, and local European regulatory agencies.

Our SAS programming staff remains continuously active in organizing and conducting educational and training activities for SAS users throughout the pharmaceutical and biotechnology industries.