Date: June 21, 2018Time: 2:30 pm EST
Research program structures vary widely among healthcare organizations. Dr. Rhonda Paz and Ms. Shirley Trainor-Thomas, drawing from their extensive..
This webinar will discuss reviewing clinical trial agreements and some of the nuances involved with these specific contracts. The clinical trial..
The Form 1572 is one of the most important documents in the clinical trial process. It serves as the one place for the most important information..
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..