Clinical Trial Design and Institutional Review Board Applications

The effort of putting together a well designed clinical trial that will support a regulatory filing for a new intended use can be a daunting task.  Oftentimes finding a place to start the process is a barrier in-and-of itself.  Bring your questions about clinical trial design, statistical methodology, informed consent, and institutional review board applications to Van Hoven Consulting to get the feedback you need.  

Contact Van Hoven Consulting today to learn more about these processes and available resources to get your clinical trial and IRB application off the ground.