Streamline your regulatory management with Forte eReg
Save time, improve workflows and enhance 21 CFR Part 11 compliance across your organization.
Learn more about Forte eReg
Improve your routing and workflows
Quickly and easily route documents, automatically alert staff when new documents are available and boost 21 CFR Part 11 compliance and efficiency with electronic signatures.
Avoid the burden of paper binders
Save time, space and internal resources by utilizing a system designed to efficiently upload, search and update documents electronically.
Apply shared documents and records across multiple protocols
Create standard templates for protocol-essential documents tailored to each study type (NIH, Industry, etc.) that can be used repeatedly, and share staff credentials across multiple protocols.
Simplify your delegation of authority process
Build a delegation of authority log to easily manage study-specific, role-based duties, and automatically route changes and updates to your PI.
Benefit from the knowledge of the Onsemble community
Forte eReg was built through close collaboration with top research institutions from across the country, ensuring that the product meets the needs of the research community.
Forte eReg FAQ
Does Forte eReg integrate with any other products?
Future integration with OnCore is planned. Any future integrations will be based on the input of our eReg customer collaborators.
How long does it take to implement Forte eReg?
The product is hosted by Forte, and requires minimal customer IT resources for implementation. This streamlines the implementation process and allows you to see value from the system in a very short timeframe.