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.
Learn how a CTMS can help you beat these common struggles and increase productivity at your clinical research site.
How varying protocols and operations should change your organization’s approach to handling external data in your EDC system.
Forte and ACRP partnered to conduct a survey analyzing the factors that contribute to technology competency and how sites, technology providers and clinical research professionals can work to improve these competencies across the industry.