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.
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.
While our industry has made tremendous progress towards improving operational efficiency, we can still do more. Taking a practical, realistic look at the tried and true CTO management methods we use every day can help us understand how to move our industry forward.
How Managed Infrastructure Can Provide a Secure, Sustainable Foundation for Your Research Technology
Utilizing a vendor-managed infrastructure can help you maximize internal resources, improve technical support, boost security and improve user experience for your enterprise software.
At last week’s 2019 Spring Onsemble Conference, we shared progress we’ve made for customers with Forte products and services, as well as the Onsemble Community’s progress toward connecting key industry stakeholders.
In this webinar, Teri Grieb of the University of Michigan will discuss how, leaders, faculty and staff came together to redesign the organizational and operational model for clinical trials at U-M by taking a systems-based approach, and how you can use some of the same principles to enact meaningful change at your institution.
Integrated research systems can help streamline your operations, centralize workflows and reduce effort across your teams. But choosing your technology providers can have a big impact on long-term success at your organization.
We are actively working on several initiatives that will create breakthrough efficiencies within individual Sites and also between Sites and Sponsors.
The Trial Data Exchange will build a two-sided network, allowing sites and sponsors can easily access and share standardized clinical research data, including critical regulatory documents.
Learn how clinical research sites can take control upfront to ensure they can be successful on the clinical trials they open.