CDSL Biostatistics Services
Bringing together the highest qualified biostatisticians, sophisticated biostatistics tools and fail-safe analytic strategies to answer the vital questions in clinical research and development.
The CDSL Biostatistics team comprises of very experienced and expert statisticians who can handle very specific statistical requirements for your study including, but not limited to,
- Design/plan Randomization
- Sample size calculation and power analysis
- Preparation of Statistical Analysis Plan (SAP) and TFLs
- Adaptive and Bayesian designs
- Patient Reported Outcomes (PRO) to Support - Medical Product Labelling Claims
- Integrated summaries of safety & efficacy (ISS/ISE)
- Descriptive and inferential methods, regression modelling and propensity scores
- Design complicated statistical analyses and imputation methods like Mixed Model for Repeated Measures (MMRM) and Multiple Imputations (MI)
Our experienced biostatistics team works in all phases of clinical trials from pre-clinical analysis to post-marketing support. We will collaborate with your research and management team and be actively engaged throughout the trial. Our foremost goal is to deliver high-quality work on time. Every project is closely monitored for methodology, employing internal procedures that guarantee complete accuracy and precision of results.
Whether it is statistical consultancy or hands-on statistical design and programming work, CDSL can support you, call us today!
