Knowing how to effectively research and develop a protocol is essential to the market approval of a clinical trial. In writing protocols, researchers engage scientists, HCPs, project managers and patients as each perspective makes an important contribution to the work being done.
In the following case study, we illustrate how a global pharma company was able to gather patient feedback about significant protocol data in order to render a positive impact on a clinical trial.
Being somewhat blinded and allowing everyone to answer promotes actually getting advice from advisors. Often times in real person advisory boards, a few of the advisors dominate the meeting and many are afraid to speak or too shy to speak. This forum overcomes many of those barriers.Within3 Participant