Moore Co-Authors Chapter on Federal Oversight of Pharmaceutical and Medical Device Marketing

Shook, Hardy & Bacon Pharmaceutical and Medical Device Litigation Associate Timothy Moore has co-authored a chapter on U.S. Food and Drug Administration (FDA) and Federal Trade Commission (FTC) oversight in the second edition of Pharmaceutical and Medical Device Law: Regulation of Research, Development, and Marketing (Bloomberg BNA and American Bar Association 2016). In "Federal Regulation of Advertising, Promotion, and Distribution Practices," Moore discusses "FDA’s prescription drug advertising regulations, FDA’s regulation of over-the-counter (OTC) drugs, and Supreme Court rulings on federal preemption of state law-based tort actions for OTC drugs, prescription drugs, and medical devices." The volume also covers the regulation of dietary supplements, ethics in research and the rules applicable to pharmaceutical compounding.