Resources
Join us at the industry’s first conference for clinical research site leaders (e.g., presidents, site directors, deans and clinical research office directors), along with the most engaged Site Council supporters and partners. Attendance will be limited. To learn more, contact us at support@sitecouncil.org.
The Site Council’s 4,000-member LinkedIn group is a forum for sharing practical solutions to the problems that face clinical research. To join the discussion, click here
To download the Site Council Dream, click here. To download a flyer, click here.
Search 11,089 FDA answers to questions about Good Clinical Practice regulations and guidelines, as well as 202 clinical investigator warning letters. To find answers to your questions, click here.
FMV concepts actually justify high budgets for high-performing sites. Instead, study sponsors and CROs often misuse them to negotiate study budgets down to commodity levels. To view an article that reveals how FMV actually works, click here. To view an article about objectively calculating FMV based on a site's performance, click here. To view an FMV legal opinion letter, click here. To obtain an FMV toolkit, contact us at support@sitecouncil.org.
The Clinical Research Interoperability Standards Initiative (CRISI) is developing a library of standard data elements so the technologies that sites choose to use can talk to each other and to sponsor and CRO technologies. To learn more, click here.
Has a study sponsor ever notified its sites that obsolete study records may be destroyed? Apparently not, and that’s why study sites are storing countless boxes of obsolete study records. What a pointless waste. To view an article that addresses this problem, click here. To view additional material, click here.
In today’s environment of high interest rates, the cost of carrying accounts receivable is a heavy burden. How is it impacting your site? What can you do about it? And why are payments so slow, anyway? To learn more, click here.
