An experienced CRA may follow all the rules and requirements for writing a site monitoring visit report (SMVR), but there are nuances that can make the difference between a report that simply follows that formula and one that really paints a picture its audience can understand. Read More
Clinical trials can’t focus on everything when it comes to process improvement, so sponsors and sites need to focus on critical success factors, such as data reliability and protecting subjects. Read More
At its very core, a clinical trial is a measurement system. But unlike other fields that rely on measurement and data reporting, the clinical trials industry has not focused enough on training for everyone involved, from the investigators all the way down to the patients. Read More
A report from IQVIA has identified eight drivers of clinical development the company says will reach “peak impact” over the next two to four years. Read More