The 2019 PRIM&R AER Conference provided insights into the changing regulatory world, and reaffirmed the importance of technology as processes and regulations continue to evolve.
Effective budget negotiation is consistently a hot topic for clinical research sites. Here are a few tips to make sure your site gets the most from your negotiations.
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.
Demonstrating the value of your research is key for securing grants and other funding. Here are a few question you should be asking.
Learn how an eRegulatory-CTMS integration can improve workflows and bring additional benefits to your institutional research operations.
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.
From ‘the professional research subject’ to ‘how to be patient-centric with payments,’ here’s a roundup of the latest posts on clinical trial compensation.
When Wayne State University (WSU) wanted to take on more IND and IDE trials, they chose Forte EDC and Forte’s Validation Service to help streamline the process.
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.