At this year’s CCAF conference, we will host a pre-conference workshop, “Research Administration Technology Workshop”, allowing us to work collaboratively with the clinical research community.
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.
Forte’s director of product management attended the SCDM Annual Conference earlier this month, and took the time to reflect on the growth of the clinical data management domain.
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.
Leveraging technology is essential to successfully streamlining the start-up and conduct of trials. From clinical trial management systems to electronic regulatory management systems, clinical research technology has been instrumental in making improvements in the entire protocol lifecycle.
In this webinar, members of Forte’s project and product management teams will provide a roadmap to ensure your site is following best practices for collecting and making the best use of your data.
Learn how UChicago decided to make the move from a custom application to a community and vendor supported solution to manage their research administration data. UCCCC chose to leverage EVAL as their first Forte solution to help streamline their data management processes.
Creating processes that result in accurate, timely and complete data are invaluable when implementing or optimizing a CTMS. Here are a few tips to achieve your goals.