* Our functinal teams include medical monitoring, clinical operations, project management, data
management, biostatistics, regulatory affairs, and QA.
* 40+ professionals with years of extensive experience in
drug/medical device clinical trials
* SFDA key advisory panel members for CTA/IND, NDA/PMA
application review
* Author of statistical subsection for SFDA Clinical Trial Guidance
and SFDA staff training
* Collaborative experience with global CROs & pharma
* Authorship of more than 10 SFDA statistical guidelines