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 » Clinical Investigator Warned for Informed Consent Failure
Clinical Investigator Warned for Informed Consent Failure
January 8, 2010
Thomas Gazda, a principal clinical investigator of a pediatric study, has received a warning letter from the FDA for failing to follow protocol regarding
informed consent and monitoring of patient compliance, which raises questions about the trial’s data.