FDA District Office meeting
This article was originally published in The Gray Sheet
Executive Summary
Scheduled for July 17 in New Orleans to discuss "good clinical practices in investigational product research." Topics to be discussed are requirements for conducting investigational research and "practical issues," including how to prepare for a data audit and what to expect during an investigation. The meeting is formatted for open dialogue between FDA and individuals involved in investigational product research. First priority for attendance will be given to individuals located in Louisiana and Mississippi. Call Rebecca Asente at 504/589-6344, ext. 158, for additional information...