This is a partial summary of our capabilities:

   Adaptive and fixed designs
   Statistical modeling
   Statistical programming and software development
   Clinical trial simulation
   Decision analysis and development strategies
   Report to and participate on Data Monitoring Committees
   Bayesian hierarchical modeling
   Bayesian meta-analysis, including network meta-analysis
   Bayesian survival analysis
   Longitudinal models for early endpoints, biomarkers, etc...
   Selecting prior distributions
   Dose escalation and dose finding
   Creating formal study protocol
   "Bridging" trials that share a single arm
   Develop custom statistical software for designs
   Predict outcomes of trials comparing new and/or existing therapies
   Support and design trials for grant-funded programs and groups
   Experience with FDA and EMA, and presenting to advisory panels