Understanding why patients say yes to being part of a clinical trial is important information that can help you craft enrollment strategies. Because you..
The confidentiality disclosure agreement (CDA) is often the first official step in the trial procurement process. Once a trial sponsor – CRO, pharma or..
Dr. Rhonda Paz’s recent webinar, “Run Your Research Program as a Business: 6 Techniques to Grow Your Site,” with Forte Research Systems drew more than..
We hope to see you there! GuideStar’s Trial Pipeline Manager, Manda Materne, will be speaking at MAGI East 2016 on Monday May 2, 1:30 pm – 2:15 pm.
Dr. Rhonda Paz, GuideStar’s Chief Operating Officer, strongly believes that clinical research programs should be operated like a business. Forte recently..
Two of GuideStar’s experts share the qualities and best practices of successful community research sites.
Is your research program functioning on dozens of Excel spreadsheets? A clinical trials management system (CTMS) can bring significant time and resource..
The Alliance for Clinical Research Excellence and Safety (ACRES) and GuideStar to partner on site-sustainability standards, global site network..
We recently asked you to tell us what your number one study start-up challenge is—and boy did we hear!