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.
We work with a wide range of Pharmaceutical and Clinical Research Organizations from all over the world.
Our dynamic structure allows us to be flexible to meet the various needs of our clients, and our varied experience ensures the advice and service we provide is amongst the best in the industry.
We are proud that most of our work is repeat business, demonstrating our commitment to clients, and their confidence in us producing the deliverables on time and to a high quality.
"Shafi did some very complex and important data transformations for us for high profile multiple trials. He managed the communications between the functions as well as the validation of the programming with his team during these very tight timelines. He was able to coordinate this communication between multiple countries and come up with creative solutions with the team to complete the job on time. We will be happy to consider Shafi Consultancy again in the future."