*  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
Faster Development
Through Emerging Markets
Copyright 2012 Truevic