Cro services

​Our services in Clinical Trial reporting include:

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• Trial design, power calculation and randomisation lists
• Input to protocol
• Statistical analysis plan, including shells
• Data loading from a wide range of formats
• Statistical programming by SAS certified professional
• CDISC SDTM and ADaM compliance

• End-of-text Tables, Figures and Listings in MS Word compatible RTF, DOCX and PDF-formats
• In-depth exploratory analysis
• Graphical presentations
• Statistical reporting, which includes all SAS programs and macros as required by authorities

We also provide on-site contract consulting in biostatistics and statistical programming and serve as DSMB/DMC Statistician.