statistical design, analysis and reporting

"A combination of knowledge, experience and dedication."

Cmed provide a complete statistical service. Our approach is client-oriented, providing a timely and quality product. Our commitment to service derives from our efficient processes supported by a specially developed, regulatory-compliant, global statistical programming environment using SAS version 9 and, as importantly, our experienced biostatistical and statistical programming teams.

Growing in strength each year, Cmed have successfully undertaken a variety of statistical and reporting tasks from individual studies to whole projects and regulatory submissions. With our latest internal quality procedures receiving positive feedback from auditors and our dedicated, hardworking individuals prepared to make your priority, their priority, Cmed are confident of meeting or exceeding your expectations.

We provide the following services:

• Protocol and CRF development
• Sample size calculations
• Randomization generation
• Statistical consultancy
• Statistical analysis
• Analysis, tables, figures and listings programming
• Statistical reporting
• Overall summaries of safety and efficacy
• Data Safety Monitoring Board support
• Interaction with regulatory authorities
• Design, analysis and reporting of adaptive design trials

Our experience and knowledge ranges from Phase I to Phase IV, across a comprehensive portfolio of therapeutic areas, most notably in the oncology area. We also have expertise in bioequivalence, drug-drug interaction and pharmacodynamic studies, including PK modelling.