CRC Pharma’s biostatistics and statistical programming team provides world-class, regulatory compliant and integrated solutions, through our relevant expertise of programming and extensive experience of statistics. A right analysis of the right data, using right methods leads to right conclusions for any clinical study which would have translational impact on getting safe medicines to the public. Hence, we believe in providing scientific and rational solutions through operational support as well as strategic advice. We have capabilities to extrapolate our resources to meet the peak demands and provide dedicated teams. Our experts work with science driven and passionate clients in a team based fashion to provide applicable and reliable solutions. We work with them to determine appropriate methods for collecting, analyzing and presenting data while maintaining high compliance with regulatory guidelines and current practices in the industry. Our expertise spans across the translational spectrum ranging from preclinical to early and late phase clinical development.

Our programmers create study specific, need based, customized outputs with their adaptability to accustom to the clients specific requirements. We achieve this systematic statistical data analysis with careful, factual planning considering all the potential fluctuations in the real life scenario. Our team members are intricately involved throughout the lifespan of a project.