We believe that clinical trials can perform better than they normally do!
The key to this is a careful analysis of the trial sites’ recruitment potential and of all the clinical trial processes in regards to their feasibility, as well as good relationships and trustworthy collaboration with the investigators.
With a Clinical Trial Liaison Team, you can achieve that. We will be happy to show you how we proceed on this. [More ...]
With our High Quality Monitoring we ensure the correct execution of all study-related tasks, which have to be completed by the study teams of clinical trial sites in the course of clinical studies from initiation to close out, and reach the goal of any-time „Inspection Readiness“ of the clinical trial sites participating in the studies.
Biopharmaceutical and medical companies thus avoid the increased personnel resources for preparing audits and inspections and the associated costs for the later implementation of Corrective and Preventive Actions CAPAs. [More ...]
And our Clinical Trial Task Force masters unplanned or unplannable operational challenges of your clinical studies. [More ...]