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 » Investigator Warned Over Improper Patient Reports
Investigator Warned Over Improper Patient Reports
February 13, 2015
The FDA warned a Phoenix, Ariz., clinical investigator for confusing audiometry reports for patients taking part in a clinical study of Purdue Pharma’s hydrocodone bitartrate painkiller.