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Zeesta is designed to meet the rigorous demands of modern clinical trials, offering a suite of tools that are both powerful and intuitive. From initial trial design through to data archiving and analysis, our platform supports your entire workflow, ensuring accuracy, efficiency, and regulatory compliance every step of the way.
Study Dashboard: Customisable dashboards offer real-time insights into trial progress, participant status, and key performance indicators (KPIs), all in one centralised location.
Site and Team Management: Oversee multiple study sites, manage user roles, and coordinate teams with permissions management and secure access controls.
Document Management: Simplify document handling with our integrated eTMF system, featuring auto-naming, version control, and secure e-signatures for compliance and audit-readiness.
Flexible Data Capture: Collect data in various formats, including text, numeric fields, images, and videos. Benefit from features like field dependencies, derived fields, and automatic calculations.
Task and Visit Scheduling: Plan and manage participant visits, tasks, and milestones with a flexible, easy-to-use scheduling tool that keeps your trial on track.
e-Consent and ePRO Integration: Enable participants to sign consent forms electronically and complete patient-reported outcomes (PROs) through a user-friendly interface.
Randomisation Engine: Deploy complex randomisation strategies with support for stratification and block randomisation, ensuring balanced treatment assignment.
Supply Chain Management: Track and manage trial supplies, including drug inventory and device allocation across multiple sites.
Configure your study as site-based, decentralised, or hybrid.
Real-time Communication: Provide participants with direct access to study coordinators via secure messaging, notifications, and task reminders.
Personalised Participant Dashboard: Offer a personalised experience where participants can track their own progress, view upcoming tasks, and access study information.
Automated Alerts and Notifications: Configure custom alerts for data queries, safety issues, or suspicious activity, ensuring timely interventions and data integrity.
Safety Data Monitoring: Monitor adverse events and other safety data with configurable thresholds, automatic notifications, and detailed reporting.
Data Validation and Quality Assurance: Ensure high data quality with built-in validation rules, automated query generation, and compliance with industry standards like CDASH 2.0.
Secure Document Storage: Store and manage all trial documents within our compliant eTMF system, ensuring everything is organised, secure, and accessible.
Workflow Automation: Automate document workflows, including approvals, e-signatures, and version control, to streamline the document management process.
eCentralised Project Tracking: Track all project milestones, deliverables, and timelines within a single, centralised module that integrates seamlessly with other platform features.
Team Collaboration: Foster effective communication and collaboration with integrated messaging, forums, and task management tools.
EHR Integration: Seamlessly connect with Electronic Health Records (EHR) systems to streamline data collection and reduce manual entry errors.
Third-Party Services: Easily integrate with other essential third-party tools and services, ensuring your trial is connected and efficient.
Custom Workflows and Configurations: Tailor the platform to your study’s unique needs with flexible workflow configurations and custom feature sets.
Scalable Infrastructure: Handle studies of any size or complexity with our scalable cloud infrastructure, designed to grow with your needs.