The 11th annual AACI-CRI conference is quickly approaching, drawing academic clinical research leaders from across the country. We preview some of the key focus areas of the 2019 conference.
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.
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.
Three key reasons why vendor-provided hosting and infrastructure could be a more sustainable solution for your clinical research software.
Implementing change can be a difficult and time-consuming experience for clinical research leadership. Here are a few tips to make the transition easier for your teams.
Learn how a CTMS can help you beat these common struggles and increase productivity at your clinical research site.
This Clinical Trials Day, we want to celebrate the contribution made by your clinical research coordinators, and provide actionable ways to provide them with a fulfilling work environment.
How varying protocols and operations should change your organization’s approach to handling external data in your EDC system.
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.
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.