In addition to our pre-study planning and mid-study statistical support services, we offer comprehensive analysis of your study data. Once your data are collected, our expert biostatisticians analyze and interpret the results, which are fully documented and verified. Regardless of how complicated the data, we can devise and implement an appropriate analysis plan. Our post-study biostatistics services include:
Analysis and interpretation of data from:
Clinical trials (Phase I-IV)
Observational studies
Patient registries
Claims databases
Surveys
Chart abstractions
Integrated summary of safety (ISS) reports
Integrated summary of efficacy (ISE) reports
Systematic reviews and meta-analyses
Safety analysis and signal detection
Quality of life (QOL) analysis, including quality-adjusted time without symptoms of disease or toxicity of treatment (Q-TWIST)
Statistical programming
Results section write-ups (including tables, listings and graphics) for final study reports, investigational new drug applications (INDs) and/or new drug applications (NDAs)
We are experts in standard and complex analytical techniques, including propensity scoring, multiple imputation and sample weighting, and our services are ICH GCP-compliant, which means you can confidently rely on the results from our statistical analyses.
