Press Release
Issa, Jordan, Woodall Probe FDA’s Giveaway to Trial Lawyers
“FDA developed the proposed rule to ensure manufacturers of generic drugs would face liability, and resulting litigation, by establishing a process for generic drug manufacturers to change their label without prior FDA approval,” the lawmakers wrote in the letter. “It seems to us that the proposed rule is not designed to address a health or safety related concern, instead it is designed to placate special interests groups and increase lawsuits.”