“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
See how Wayne State University used Forte EDC and Forte’s Validation Service to boost their 21 CFR Part 11 compliance for FDA-regulated IITs.
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.
Minimize duplicate data entry using the lab results interface
Pull lab results, unit, and low and high normal ranges into lab CRFs from your source system via FHIR.
Streamline workflows by leveraging OnCore CTMS integration
Take advantage of Forte EDC’s integration with OnCore CTMS to pull information related to Organizations, Protocols and Subjects.
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 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, integrates with OnCore CTMS, and offers a lab results interface via FHIR.
Who hosts Forte EDC? Does my IT Team need to be involved?
Forte EDC is an easily accessible, cloud-based, Forte-hosted solution. 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 can I validate 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 service. Our holistic approach encompasses implementation and initial validation.
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.