As a therapeutically-focused Clinical Research Organization (CRO), we approach our Clients' work with extensive medical and regulatory expertise in delivering additional input, strategy, and efficiencies to each and every phase of the clinical trial thus reducing the time, risk and cost associated with conducting Clinical Trials while maintaining highest levels of Quality, Execution and Delivery.

We place a high value on relationships – with our Sponsors, our investigators and sites, and our patients – and seek to establish long-term partnerships. Our focused and experienced teams in concert with management across the globe provide unrivaled support at every stage of the drug development process that too, scientifically, ethically and reliably in compliance with GCP guidelines and maintaining the most stringent norms of Data integrity and confidentiality.

One size does not fit all, thus we ensure every Sponsor receives personalized service. Sristek can provide tailored made end to end solutions to any aspect of clinical research, clinical data management, biostatics, Medical Affairs and Pharmacovigilance at significantly lower overheads and cost advantage. Sristek excel in conducting multi-center, multi geography clinical trials as well as functional service provider model for clinical data management, statistics, programming, medical writing and pharmacovigilance projects.