Advarra stands with the research community during this crisis. Here are just a few of the many ways we can help you prepare for the new clinical trial landscape. If your institution needs help restoring your research in the wake of COVID-19, fill out the form to get started. An Advarra representative will contact you to discuss next steps based on your institutional needs.
- SOP Design, Administration, and Compliance
Work with our proactive, collaborative consulting team to evaluate how COVID-19 has affected your study conduct and build new processes for your research operations moving forward.
- Staff Augmentation Services
Ensure your clinical research operations continue to run smoothly with expert business analysts, project managers, IRB support, and technology support staff.
- Free Transfer of IRB Oversight
To prevent COVID-19-related challenges from leading to unnecessary study closures, Advarra is offering free transfer of IRB oversight through the end of 2020. Advarra will oversee the transferred studies and sites until your original IRB is prepared to re-take the research.
- Free eRegulatory Management System
Streamline remote regulatory workflows and enable remote monitoring access with a free version of Forte eReg software—eReg Lite—available for the remainder of 2020. eReg Lite provides many features that enable virtual telework and collaboration such as remote monitoring capabilities, electronic signatures, and delegation of authority.
- Free Business Operations Services (BOS) for COVID-19 Studies
For current technology customers, Advarra is offering complimentary study calendar builds, budget setup services, and coverage analysis services on COVID-19-related studies. Our BOS team provides expertise to ensure your COVID-19 studies are activated quickly, easing the burden on your team.