Genpro Research Information

Genpro bring together the global best practices in clinical data management, biostatistics and programming and deliver cost effective solutions to our clients with utmost quality. We are an organization cofounded by a team of very experienced biometric professionals and funded with a vision to technologically augment the clinical trials. We are just beginning our pursuits and have very fast and ambitious scale up plans. You will be compensated as per the industry standards and will be provided with an excellent work life balance here at Genpro. Genpro offers expert consulting services on complex statistical issues encountered during study design or analysis. We provide guidance in incorporating and analyzing the effectiveness of statistical methodologies in clinical trials with a great deal of expertise in adaptive designs and Bayesian analysis. Our biostatisticians possess the experience and critical thinking to assist clients. They are industry experts in several statistical areas including adaptive design, personalized medicine, Bayesian analysis and non-inferiority approaches with extensive experience in several indications. Genpro team has been working for more than 15 years in NDA/ BLA/PMA submission and interacting with FDA/ EMEA and PMDA and actively collaborate with academic, industry and FDA working groups. We are well versed with CDISC data standards and electronic submission standards to deliver high quality, dependable analyses.