See the results of Forte’s survey of over 120 representatives from clinical trial sites and sponsors on the causes and challenges of extremely delayed clinical trial payments.
Learn how sites can quantify protocol complexity and anticipate resources to ensure more efficient clinical trial processes.
Principal Investigators are responsible for the compliant and efficient execution of a clinical trial. How can a research organization empower investigators with the tools and information to maximize their success?
Workshop discussion reveals common struggles and creative solutions for communicating with PIs about site financials.
Earlier this year we published a state of the industry report, highlighting some of the key challenges shared among more than 900 clinical research professionals who participated in our survey. The results of the survey weren’t surprising to us – there’s enormous opportunity for growth and improvement across all facets of clinical research operations. To…
Join us at 2017 MAGI West where Forte team members will present on research operations improvement, technology roadmaps and site payments.
Use these six simple steps to implement effort tracking at your clinical research site.
Knowing when to delegate a task to qualified research staff isn’t always straightforward. Learn why navigating the gray areas of delegation of authority can be particularly problematic.
Use these free resources to learn the research impacts of NCI designation and the necessary steps for successful CCSG approval and renewal.
Many research sites lack the right data to understand their performance, but tracking metrics helps turn insight into action to bring forth improvements.