We provide comprehensive data management services for phase I-IV clinical trials and pharmacovigilance. Our goal is to transform raw data into consistent, accurate, reliable, meaningful trial output in full compliance with regulatory guidelines. Our endeavour is to reduce time between last patient last visit (LPLV) and the database lock, meeting quality benchmarks. Our services span every phase of the drug development pipeline. The team has extensive experience in handling studies with EDC requirements. We have been exposed to eTMF, eISF, ePRO and other CTMS tools.

Our business delivery model complements exceptional quality, project management and visibility that are essential for success of complex global projects. We understand the intricacies of transition projects and our clearly defined process guidelines emphasize the importance of information flow and communication. We provide sponsors with integrated solution of various service components accessing extensive global network of resources, technologies, facilities and processes to efficiently, consistently and rapidly address sponsors unique needs.