Headed by Mihir Gandhi

Our highly qualified and experienced biostatisticians and epidemiologists help you with protocol development by navigating the complexities of study design, sample size, randomisation, database standardisation and statistical analysis methods. The team also provides statistical report writing, research manuscript preparation, interim and final analyses. These recommendations have frequently led to high quality deliverables with great efficiency in time and costs. The scientists also support investigators in regulatory approvals and grant proposals. Leveraging biostatistics in the planning stages of the study design, SCRI helps you to accelerate timelines, improve cost effectiveness and quality of the clinical studies. The team has extensive clinical research experience in phase I to III clinical studies. All team members hold advanced degrees (Masters and PhD).