Statistical Programming

As BDM’s core function, statistical programming team is built upon a group of energetic young professionals with excellent programming skills and solid statistical knowledge. Closely collaborating with biostatisticians, our programming has been supporting data analysis for clinical trials at different stages of drug development including early phase clinical trials (FIH studies, phase II proof of concept studies) phase III registration trials and post marketing studies such as observational studies. The focus of programming effort is on both creating CDISC-compliant and submission-ready datasets and documentations along with statistical tables, listing and graphs for clinical trials and performing complicated exploratory data analysis to support commercialization effort of the clients. Being part of expanding global biometrics team of over 600 professionals, we have demonstrated on-time delivery of high quality work for meet urgent request and rapid scalability to handle a large amount of work with the tight timeline.

Our services

  • Legacy data conversion
  • Implementation of statistical methods to overcome the challenges of clinical research
  • CDISC-compliant datasets and electronic submission packages
  • Programming support the submission based on health technology assessment
  • Data visualization
  • Data analysis of healthcare databases in support of health outcome research.