Next-Gen eSolutions Platform for Sponsors, CROs, and Clinical Sites
Simplifies & Optimizes the
Clinical Trial Workflow Ecosystem
Our Clinical Trial Ecosystem
Powerful applications designed to support every stage of your clinical trial operations.
SPONSORs/CROs
Centralized dashboard for managing studies, sites, budgets, and performance insights.
Site
Tools for site teams to manage studies, patients, documents, and communications.
eCLINICAL SOLUTIONS
Optimize Your Clinical Trial Ecosystem
Managing clinical trials requires precision, coordination, and real-time visibility. Our integrated ecosystem empowers sponsors and site teams with the tools they need to streamline operations, enhance collaboration, and drive better outcomes. From study planning to execution, ensure every phase is efficient, compliant, and data-driven.
Sponsor/CRO
Centralized dashboard for managing studies, sites, budgets, and performance insights.
Site
Tools for site teams to manage studies, patients, documents, and communications.
Advancing Clinical Research With Unified,
Paperless Technology Ecosystems
Today’s clinical trials demand speed, accuracy, and total efficiency. COSMOS replaces paperwork, delays, and scattered systems with one
unified digital platform—empowering Sponsors, CROs, and Sites to work smarter, faster, and more collaboratively.
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Solutions for Sponsors & CROs
Faster Study Activation. Stronger Compliance. Better Trial Outcomes
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.
Initra – SSU
Accelerate study activation with streamlined workflows, automated document management, and intelligent site identification tools that reduce delays and improve efficiency.
TrialOps
Manage clinical trial operations with real-time visibility, centralized collaboration, and simplified tracking of site performance, milestones, and compliance activities.
FinTrial
Automate investigator payments with transparent tracking, accurate calculations, and faster processing to ensure sites are paid quickly and efficiently.
Clyra eConsent
Deliver a modern patient consent experience with secure digital consent, improved participant understanding, and simplified documentation management.
Solutions for Sites
Run smarter, faster clinical trials COSMOS empowers sites.
From Site CTMS and eDocs to eSource, eConsent, cPAY, Digital Logs, eFax, and Trial Track, COSMOS provides a fully integrated platform to support end-to-end clinical trial operations. The unified system reduces manual effort, improves collaboration, and maintains data integrity across all study activities.
The result is more efficient workflows, faster trial execution, enhanced audit readiness, and improved coordination between sponsors, CROs, and research sites.
01
CTMS
Manage clinical trials with a centralized platform designed for research sites. Track subjects, monitor progress, manage tasks, and maintain complete visibility across all study activities.
02
eConsent
Deliver a secure and user-friendly digital consent experience. Improve patient understanding, simplify documentation, and ensure compliance with modern electronic consent workflows.
03
eSource
Capture clinical trial data directly at the source using digital tools. Reduce manual errors, improve data accuracy, and enable faster monitoring and reporting.
04
eReg
Simplify regulatory management with centralized tools for document tracking, compliance oversight, audit readiness, and secure access across all clinical studies.
05
Subject Stipend
Streamline participant payments with tools designed to manage reimbursements, track compensation, reduce delays, and improve subject satisfaction efficiently.
06
TrialTrack
Monitor clinical trial operations with real-time tools for study tracking, milestone oversight, site performance monitoring, and operational visibility.
01
CTMS
Manage clinical trials with a centralized platform designed for research sites. Track subjects, monitor progress, manage tasks, and maintain complete visibility across all study activities.
02
eConsent
Deliver a secure and user-friendly digital consent experience. Improve patient understanding, simplify documentation, and ensure compliance with modern electronic consent workflows.
03
eSource
Capture clinical trial data directly at the source using digital tools. Reduce manual errors, improve data accuracy, and enable faster monitoring and reporting.
04
eReg
Simplify regulatory management with centralized tools for document tracking, compliance oversight, audit readiness, and secure access across all clinical studies.
05
Subject Stipend
Streamline participant payments with tools designed to manage reimbursements, track compensation, reduce delays, and improve subject satisfaction efficiently.
06
TrialTrack
Monitor clinical trial operations with real-time tools for study tracking, milestone oversight, site performance monitoring, and operational visibility.
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Click on the below link to request a demo
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