What is ImproWise?
ImproWise is an all-in-one web-based platform designed to streamline clinical trial management and clinical data management. It combines CTMS, CDMS, EDC, CTBM, CTPM, eTMF, ePRO, and RBACS functionalities into a single integrated system, providing end-to-end management from planning to close-out. The platform offers real-time analytics, automated workflows, and comprehensive audit trails to enhance efficiency and ensure data accuracy.
Built with a focus on security and compliance, ImproWise is HIPAA compliant and features a dynamic, database-driven system that requires minimal customization. It supports multi-trial and multi-site management through a single login, with user-friendly tools like dynamic eCRF design and flexible query builders accessible to non-technical staff. The platform is scalable and configurable to meet unique trial requirements while maintaining data integrity and regulatory standards.
Features
- Multi-Trial, Multi-Site Management: Capable of managing multiple trials and sites through a single login simultaneously
- Dynamic eCRF Design: Ability to design electronic Case Report Forms dynamically on the fly within days
- Real-Time Analytics: Provides instant access to trial data for informed decision-making
- HIPAA Compliant: Ensures compliance with data security and privacy standards
- User-Friendly Query Builder: Flexible query builder accessible to non-technical staff without programming knowledge
- Comprehensive Audit Trail: Audit trailing for every data element entered and changed to ensure data integrity
- Clinical Data Management System (CDMS): Delivers reliable data integrity with automated reconciliation and traceability
- Clinical Trial Budget Management (CTBM): Offers total financial control with accurate budget management and payment tracking
Use Cases
- Managing end-to-end clinical trial lifecycle from planning to close-out
- Streamlining clinical data management with automated reconciliation and traceability
- Budgeting and financial oversight for clinical trials
- Storing and managing clinical trial documents in a secure electronic trial master file
- Designing and customizing electronic Case Report Forms for specific trials
- Monitoring trials in real-time with analytics and reporting
- Ensuring compliance with HIPAA and other regulatory standards
- Collaborating across multiple sites and teams in clinical research
