Brochure | January 27, 2021

Advarra eRegulatory Management System Overview

Source: Advarra

Think beyond the binder

Managing essential clinical trial documents at academic medical centers, cancer centers and health systems is often an exhaustive, extremely manual process that requires both physical storage space and site resources. The Advarra eRegulatory Management System (Advarra eReg) provides integrated protocol, staff and institution documentation to streamline regulatory process and enhance compliance.

Advarra eReg takes a templated approach to creating and maintaining electronic binders. This is ideal for academic institutions managing a large number of protocols. Moving key regulatory tasks to the system level—instead of the protocol level—eliminates redundant workflows, boosts compliance and saves valuable staff time. Combined with 21 CFR Part 11-compliant electronic signatures for protocol documents, delegation of authority, and more, the system significantly reduces the regulatory burden for your staff.

Streamline your regulatory process and think beyond the binder. Save time, improve workflows, and enhance regulatory compliance across your organization with a system designed for academic institutions managing a large volume of protocols.

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