TryAll CTMS
Solution Overview
TryAll CTMS is a Clinical Trial Management System that streamlines trial management, ensures financial control for timely sponsor invoicing, and provides KPI monitoring for research centers, including trial count, associated value, response times, and patient involvement.
Key Features
Problems Addressed / Key Features:
- Fragmented Processes: Centralizes all clinical trial management activities in one platform.
- Delayed Financial Tracking: Provides real-time financial control and ensures timely invoicing to sponsors.
- Lack of Visibility: Offers dashboards and KPIs for monitoring performance and decision-making.
- Rigid Market Solutions: Delivers a flexible, configurable accelerator instead of a closed product.
- Complex Stakeholder Needs: Designed to meet the requirements of clinical, financial, and management teams.
- Scalability Challenges: Built to grow with additional features like ethics approvals, drug management, and e-consents.
- Poor User Experience: Modern, intuitive interface that simplifies daily tasks and improves usability.
Key Benefits
Target Audience: TryAll CTMS is designed for all entities conducting studies and clinical trials: public and private hospitals, primary healthcare providers, biomedical research centers, academic clinical centers, and independent clinical research centers.
Key Benefits of TryAll CTMS:
- Streamlined Clinical Trial Management: Simplifies and accelerates processes across all phases, from feasibility to study closure.
- Financial Control and Timely Invoicing: Ensures accurate tracking of financial activities for prompt billing to sponsors.
- Comprehensive KPI Monitoring: Provides dashboards and alerts to track key metrics such as number of trials, associated value, response times, and patient involvement.
- Customizable and Flexible: An open, configurable accelerator that adapts to the specific needs of each research center.
- Designed for All Stakeholders: Addresses the requirements of clinical, financial, and management teams with tailored tools and insights.
- Scalable for Future Growth: Ready to integrate advanced features like ethics committee approvals, investigational drug management, e-consents, and recruitment optimization tools.
- Modern User Experience: Intuitive, visually appealing interface that enhances daily workflows and user satisfaction.