Starting a clinical trial is no simple task. From developing a protocol to patient recruitment to U.S. Food and Drug Administration (FDA) submission, there are a wide array of complex and closely monitored processes along the way. Patient and community involvement help ensure study questions are relevant and that the trial is achievable. Hear from experts on ways to partner with industry and regulatory agencies to design a clinical trial.

Speakers: Neena Nizar, Alison Skrinar, PhD, & James Valentine, JD, MHS