We provide expert data management and biostatistics solutions across the development pipeline, from phase I to Phase IV regulatory studies. We are experienced in both diagnostic and theraputic development, using both paper and electronic CRFs. Our services and solutions are covered by a comprehensive suite of standard operating procedures, and we pride ourselves on being able to combine high end statistical work using emerging clinical platforms (such a pharmacogenomics and next Gen sequencing) with tightly controlled and regulatory compliant processes.

We are also able to deliver flexible and cost-effective solutions for investigator initiated trials.