IRB-Ready™ helps condense the time it takes to obtain IRB review for numerous sites to the time ordinarily needed to approve a single site. 

Solution for Sponsors and CROs

Advarra Cloud is a next-generation platform delivering applications in an easy-to-use, fully managed environment. Powering Advarra’s Research Site Cloud and Life Sciences Cloud, it is built upon research industry best practices. Advarra Cloud meets your changing business and regulatory compliance needs, lowering your overall cost and reducing complexity.

Improve your clinical research operations strategies using comprehensive, diverse dashboards built through collaboration with top researchers.

Efficiently manage stipends and travel reimbursements across clinical trials with our automated payment system, integrated with your OnCore CTMS.

Demonstrate the impact of your research to the NCI, NIH, and your organizational leadership.

A secure patient payment system that revolutionizes the speed of payments with real-time reimbursements to prepaid debit cards, reducing fraud risk, reducing cost, and providing full oversight directly within Clinical Conductor.

Designed to allow for continuity of patient medical records to maintain the latest documentation.

An automated tracking application designed to maximize patient access to care across a variety of departments.

Centralize and simplify IRB management

Improve workflows across sites, sponsors, and CROs via a seamless solution that supports study startup and enrollment planning and tracking. Join the 225,000 researchers already using Advarra’s technology to collaborate on study startup across the globe.

Clinical Conductor is a comprehensive Clinical Trial Management System (CTMS), scalable to optimize finances, regulatory compliance, and overall clinical research operations for all types of research sites, site networks, hospitals, and health systems.

An advanced software suite designed to improve patient safety and increase quality of care for VA and surgical facilities.

Streamline processes and increase data integrity by leveraging EDC’s integration with OnCore, the leading comprehensive clinical research management system for mid-size to large organizations with complex needs.

Pre-op scheduling and real-time status tracking application that maximizes the efficiency of surgical services from check-in through discharge, including addressing timeliness issues that impact patient satisfaction.

Maximizing resources by ensuring that operation and treatment rooms are scheduled to capacity.

Enable your staff to easily capture and manage data, facilitate remote workflows, and eliminate duplicative processes, all in a 21 CFR Part 11-compliant, integrated eSource + EDC system.

Replace manual, error-prone processes with technology that automates the secure transfer of IRB-related documents directly from the Advarra® CIRBI Platform to your electronic trial master file (eTMF) without manual loading or manipulation of documents before export. 

Two-way text messaging designed specifically for sites to maximize recruiting and reach enrollment goals, while dramatically increasing retention with HIPAA compliant, trackable messaging and reminders to participants in any location.

Advarra eConsent is an electronic consenting module for research sites, designed to keep participants engaged, simplify compliance oversight, and optimize the overall quality of the consenting process.

Think beyond the binder. Save money, improve efficiency, and enhance regulatory compliance across your organization with a 21 CFR Part 11-compliant system designed to adapt to regulatory workflows for any size research site.

Providing a comprehensive patient identification system designed specifically for the Veterans Administration to maintain patient safety and overall staff and patient satisfaction.