Webinar Replay: "How much do you know about the FDA Draft PRO Guidance?”

Presented by Chad Gwaltney, Ph.D., Scientist, PRO Consulting^®

Join us for an interactive Web Seminar that will explore various elements of the FDA’s Draft Guidance on Patient Reported Outcomess (PROs) in Clinical Research. During this one hour webinar, the scientific and regulatory experts of PRO Consulting will review the answers to 10 questions often asked by clinical researchers, such as:

When are validation activities required?
What needs to be included in a cognitive debriefing report?
How is a Minimally Important Difference (MID) calculated?

RSS Feed