Clinical Trial Statistics are an integral part of any efficient clinical trial study. Our clinical trial statisticians are experienced in working with our clients to design their clinical trial, determine endpoints, provide statistical methods and sample size determinations, as well as provide quality data oversight during the program.
Our Biometrics Group has experience of clinical trials observational studies, non-interventional studies/scientific programs and full integrated analyses of programs.
Our stats group has diverse experience in generating Statistical Analysis Plans, Final/Interim Analyses Reports, ISS/ISE Summaries, Annual Reports and Safety Reviews for DSMBs. They also support the compilation of Clinical Trial Reports and Manuscripts.