As research industry professionals we need to understand why patients decide to participate in clinical trials. This insight will help shape our..
The FDA regularly visits healthcare organizations conducting research on human subjects to ensure the safety of the patients and the accuracy of the..
These days the internet is our primary source of information and with this in mind, it is important the research program has a strong presence on the..
The site selection visit gives trial sponsors the opportunity to get to know your research program and determine if it is the right fit for their..
Developing or growing a research program requires engaged physicians who are excited and involved. Compensating physicians for their time and effort..
And it can get complicated. Understanding what those differences are, ways to prevent billing compliance headaches, and assuring a streamlined approach..
A clinical trials program should be run like a business and that approach begins with solid finances. Each new trial requires careful analysis to build..
Pharmaceutical and device companies are now required to report any payments to hospitals and physicians. That includes any payments for clinical..
External IRBs can bring efficiencies to a community hospital’s clinical research program but how does a hospital decide to use an external IRB instead..
A clinical research program introduces many benefits to a hospital and its physicians, patients and community but to be successful, a solid structure..