Statistical Consultancy
Cmed CS statistical team has a broad range of experience in providing statistical consultancy for both short and long term projects in a wide variety of therapeutic areas. We match our consultants to your projects, understanding that matching skill sets to your requirements is key to a successful partnership
- Adaptive Trial Design - Design and implementation of the next generation of biostatistics, including use of WinBUGS and Brugs for Bayesian analysis and interpretation.
- Protocol and CRF (Case Report Form) Development – From preliminary review through to finalisation of documentation, we can employ a wide range of protocol development activities with input into design considerations, utilisation of statistical methodology and sample size estimation.
- Statistical Analysis Plans and Statistical Programming - We facilitate innovative statistical approaches to ensure the earliest possible technical and regulatory success.
- Analysis Interpretation and Reporting -We help ensure you make optimal decisions based on sample sizes, number of studies, analysis methods and precise interpretations of results.
- Regulatory Services- We are able to provide biostatistical support to regulatory activities worldwide, including (but not limited to) input into regulatory documents, attendance and input at regulatory meetings and advice on the appropriate structure of integrated summaries and support of all post-approval activities.
- Advisory Panel and DSMB/DMC Meetings - Our experienced team also provides statistical support and advice for advisory and data monitoring committee meetings, either as independent or DSMB/DMC core statisticians.
