We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
Accept
Home » Final PRO Guidance: Patient Input Needed in Product Development
Final PRO Guidance: Patient Input Needed in Product Development
December 11, 2009
After three years of comment review, the FDA has issued a final guidance on patient-reported outcome (PRO) instruments submitted in applications.