Many sites understand the benefits of moving from paper regulatory binders to an electronic system. But it’s also important to ensure your organization is implementing a system that will fit your regulatory workflows and set you up for long-term success.
Protocol Feasibilities are designed to help clinical research staff determine the possibility of conducting a study. Here’s how to seamlessly work an assessment in before accepting your next clinical trial.
Coordinating centers often struggle with the administrative burden of managing regulatory documents across multiple participating sites. We collaborated with our customers to address this challenge through the Forte eRegulatory Management System.
Actively participating in the clinical research community can help you address your institutions biggest challenges, while working together with your peers to truly move clinical research forward.
Good Clinical Practice benefits research in more ways than complying with the Food and Drug Administration. Learn more about why it’s important and how it helps achieve best practices of any clinical trial.
In this webinar, Kathleen O’Malley, Associate Director of Education and Training at Jefferson Clinical Research Institute and Paul Park, Manager of Clinical Research Systems at City of Hope will discuss robust strategies to drive technology adoption with an emphasis on training practices designed to prepare end users for success.