COSMOS provides technology-driven solutions that enable sponsors and CROs to simplify and optimize clinical trial operations from study startup through closeout. By leveraging intelligent automation and AI-powered insights, COSMOS facilitates identification of high-performing research sites and accelerates critical Study Start-Up (SSU) activities, improving efficiency and reducing operational delays.

From investigator training and study collaboration within TrialOps to streamlined safety acknowledgements and end-of-study documentation workflows, COSMOS reduces operational complexity while supporting alignment across stakeholders and maintaining regulatory compliance.

COSMOS FinTrial delivers comprehensive financial management capabilities, including budget creation, negotiation, site payments, and subject reimbursements—providing end-to-end financial oversight across the clinical trial lifecycle within a unified platform.

Clara eConsent offers a 21 CFR Part 11 compliant electronic informed consent solution designed to improve consent quality, support decentralized clinical trial (DCT) models, enhance ICF compliance, and promote diverse participant engagement through accessible digital consenting workflows.

The result is accelerated study activation timelines, real-time operational visibility, improved compliance readiness, and seamless collaboration across global clinical research teams.