“Forte EDC has helped us improve our data collection processes and helped to make communication more effective. The different options for building form constraints has helped us to ensure higher data quality.”
Courtney Kennedy MSN, RN-BC
Manager, Clinical Trials Applications, University of Nebraska Medical Center
Learn More about Forte EDC
Streamline staff workflows and increase data integrity
Featuring integration with OnCore, Forte EDC reduces the number of times data entry is required, which saves your site staff time, increases data integrity and allows for easier reporting across protocols.
Enhance 21 CFR Part 11 compliance
Ensure data security and integrity using audit trails and secure signatures to fully support validation and compliance with 21 CFR Part 11. Forte offers services to assist validation and materials to ensure you maintain your validation throughout each upgrade.
Manage laboratory data securely and accurately
Centrally manage reference ranges and units for a particular lab location to bypass redundant and error-prone manual entry.
Gain insight with standard and ad hoc reporting
Maximize your reporting capabilities utilizing built-in reports to track site and protocol performance, and answer any questions about your data by creating ad hoc reports via JasperReports.
Efficiently manage queries
Create both manual and auto-generated warnings and queries that empower your monitors, data managers and coordinators.
Benefit from the knowledge of the Onsemble Community
Forte EDC is developed in close collaboration with top research institutions across the country, ensuring the system meets the needs of the research community.
Save time and ensure data reliability in one easy-to-use system
Streamline data collection, management and 21 CFR Part 11 compliance using Forte EDC, an electronic data capture system integrated with OnCore CTMS, dedicated to supporting leading academic research centers, cancer centers and health systems with its familiar user interface, robust functionality, and a collaborative approach to development.
Quickly and efficiently implement and validate Forte EDC
Our goal is to quickly provide you with a validated, centralized source for all of your investigator initiated trial (IIT) data. Our holistic, 10-week approach encompasses implementation, initial validation and study build activities, with an option to include legacy form template building.
Forte EDC is designed to serve the academic research community to help address the complexities you face running Investigator Initiated Trials. In addition, Forte EDC is validation-ready and fully supports compliance with 21 CFR Part 11.
Who hosts Forte EDC?
Forte EDC is an easily accessible, cloud-based, Forte-hosted solution.
Does my IT Team need to be involved?
Because Forte hosts Forte EDC, very little IT and administration resources are required. To maximize your ad-hoc reporting capabilities, you may need a dedicated report writer.
How long does it take to implement Forte EDC?
To efficiently implement Forte EDC, validate your instance, and develop processes to maintain your Forte EDC validation for each new protocol and system upgrade, Forte has developed a robust implementation and validation process. Our holistic, 10-week approach encompasses implementation, validation, legacy form template building, and study build activities.
Forte Solutions: Working together to help you meet your goals
Combine your top-notch research teams with our software and services to streamline your operations, decrease administrative burden and move clinical research forward.
Streamline processes and increase data integrity by leveraging Forte EDC’s integration with OnCore, the leading comprehensive clinical research management system for mid-size to large organizations with complex needs.