Customize Your Clinical Study Protocol
Contact Customization
100%100%
50%50%
5years5years
Complete SOP system intimately linked with IQVIA and complying with international ICH/GCP and CDISC criteria
Excellent record of on-time, high-quality delivery with the ability of quick responses to urgent needs;
Providing the data statistics service to clinical trials in China and abroad, MRCT conducted in many countries and clinical trials requiring submission in both China and US;
Experienced in global mainstream EDC, including Medidata Rave, Viedoc, Bioknow, Zelta, etc.
Bilingual (Chinese and English) work environment covering the whole processes from project communication to result delivery, to effectively fulfill the international needs for clinical trials in China and abord and clinical trials requiring submission in both China and US.
A professional and experienced data management team (including data manager and database designer), statistician team and programmer team with backgrounds in mathematical statistics, health statistics, clinical pharmacology, etc. Our business involves phase I-IV drug & BE studies, device projects and IVD projects. We are able to provide data statistics service to clinical trials with complex designs.
