Streamline Your Regulatory Process with Forte eReg
Think beyond the binder. Save time, improve workflows and enhance 21 CFR Part 11 compliance across your organization with a system designed for academic institutions managing a large volume of protocols.
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.
Support master delegation of authority processes
Allow PI’s to standardize delegated tasks at the system level, dramatically reducing the amount of time spent routing documents.
Efficiently and compliantly manage multi-site trials
As a coordinating center, view and manage protocol documents for participating sites in an investigator-initiated trial.
Forte eReg FAQ
Does Forte eReg integrate with any other products?
Yes! Forte eReg integrates with our OnCore Enterprise Research System. 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.
Does eReg support remote monitoring?
Yes. The eReg system allows regulatory staff to generate a unique monitoring user and login, indicate the specific protocol documents and information to be reviewed and control the start and stop points for the monitoring session.