ReDA

ReDA is a cloud-based Clinical Trial Management System offered by Infonetica. It provides a comprehensive solution for managing clinical trials, including trial setup, compliance management, budget control, and performance reporting.

The system caters to organizations of all sizes, such as research institutions, hospitals, pharmaceutical companies, and contract research organizations (CROs). According to the vendor, ReDA streamlines trial setup processes by offering tools to automate workflows and customize trial protocols, consent forms, and other study documents. It also facilitates efficient site feasibility assessments and supports the management of complex organizational networks.

ReDA ensures compliance with regulatory requirements and ethical standards throughout the trial process. It provides built-in templates and tools for creating and submitting regulatory documents, tracking ethical approvals, managing participant consent, and monitoring ongoing compliance.

The system offers comprehensive budget management capabilities, allowing users to create and manage trial budgets, allocate costs, and monitor expenditures in real-time. It provides detailed financial reporting and analysis to support informed decision-making.

With ReDA, users can generate comprehensive performance reports for individual trials or across multiple studies. The system offers customizable reporting templates and dashboards to visualize trial data and key performance indicators. Researchers can schedule automated report generation and receive real-time insights into trial progress.

ReDA provides tools for efficient participant management, including recruitment, enrollment, and tracking. It enables seamless communication and collaboration with trial participants while ensuring compliance with privacy regulations.

The system seamlessly integrates with other systems, such as HR, finance, and post-award systems, streamlining data flow and eliminating redundant data entry. It ensures secure data transfer and maintains data integrity throughout the trial process.

ReDA is highly configurable, allowing users to customize workflows, forms, and templates to meet specific trial requirements. It supports multi-department or multi-funder workflows and adapts to ongoing changes in internal and external requirements.

The system facilitates real-time collaboration between researchers, enabling them to collaborate on trial documents, track changes, and provide feedback. It supports peer review processes and enables virtual meetings with committee members.