Clinical Trial Reporting
How can we help?
We have over twenty years of experience in working with clinical trial data. We have reported data from phase I to phase IV studies, registry studies and mega trials in many therapeutic areas, including respiratory and oncology.
We also provide solutions from CDISC conversion and validation to developing generic macros and template programs. When developing these, we always take into account the experience and skill set of those who will use the programs and macros we produce.
Our solutions are always provided such that they are easy to maintain and re-use again in the future, thus helping to reduce the cost and time of future studies.
Programming and validation of Tables, Listings, Figures and Analysis Datasets.
Independent QC, double programming.
Data quality and consistency checking.
Template programs and analysis macros.