Service Available
1.       Statistical analysis
­         Clinical research-related statistical consultation;
­         Clinical research-related statistical design, including design for statistical protocol, randomization, and blinding, as well as calculation of sample size;
­         Data analysis for clinical research such as bioequivalence trials and phase I-IV trials, with statistical reports that meet the requirements of the National Medical Products Administration; and
­         Interim analysis of clinical trials.

2.       Independent data monitoring committee (DMC)
­         We assemble and run DMCs for major clinical trials. As an independent third party, the DMC monitors safety and effectiveness data and conducts interim analysis to ensure the integrity of trials and protect human subjects.