Do you agree that running a clinical project is more than controlling deliverables, budget and timelines?
Our experience is that it is just as much about asking the right questions at the right time. Getting it right from the start. We at SCRO can help you with this and much more. This includes the classic tasks: submissions to ethical committees and regulatory authorities, feasibility and site selection, overall project leadership, and monitoring of all phases of drug and medical device trials. We can help you to secure results, quality and costs.