Product Overview
eClinPro CTMS is an all-in-one, cutting-edge Clinical Trials Management System designed to simplify and streamline the clinical trial process. With powerful tools for Site and Multisite Management, eClinPro ensures seamless coordination across multiple trial locations. The system includes comprehensive Accounting and Budget tracking features, as well as a Subject Visit and Stipend Tracker to manage patient visits and compensation with ease.
The Integrated Protocol Calendar allows for efficient tracking of study timelines and milestones, while the Subject Visit Tracker provides real-time monitoring of participant progress. eClinPro’s advanced Reporting capabilities offer valuable insights into budgets, recruitment, study progress, and more, ensuring full visibility throughout the trial.
The Patient Recruitment Module aids in optimizing participant enrollment, and the “My Tasks” feature ensures that all team members stay on track with their responsibilities. Additionally, eClinPro CTMS supports smooth Data Migration, making it easy to transfer your existing data into the system with minimal disruption. Designed to boost efficiency and enhance accuracy, eClinPro CTMS is the ultimate solution for managing clinical trials from start to finish.
Deployment
- Web based
- Cloud Hosted
Pricing
- Subscription
- License Fee
- Usage Rate Pricing
More Information
- Centralized Management: A CTMS allows for the centralization of all study-related activities, including participant tracking, regulatory documentation, and financial management, ensuring that all critical information is easily accessible.
- Enhanced Efficiency: Automating manual processes and streamlining workflows reduces administrative burdens, allowing research teams to focus on the study’s quality and progress rather than time-consuming tasks.
- Real-Time Data Access: With real-time data entry and reporting, a CTMS provides up-to-date information, enabling faster decision-making and more efficient trial monitoring.
- Compliance and Regulation: A CTMS helps ensure adherence to regulatory standards, minimizing the risk of non-compliance and helping maintain high levels of quality and oversight in clinical trials.
- Cost Reduction: By improving efficiency and reducing errors, a CTMS can lead to significant cost savings throughout the trial process.
- Improved Transparency: With all aspects of the study centralized, there is increased transparency, which enhances collaboration among research teams and stakeholders.
About the company
eClinPro, LLC is an American company with a SaaS workflow for the clinical research industry providing powerful tools as CTMS/ eSource/ eDocs/ Text that facilitate the clinical trials conductions improving compliance and efficiency.
