Summary
Food and Drug Law Institute's Introduction to Drug Law and Regulation will explore the essentials of drug law and regulation and give a comprehensive understanding of the administrative agencies that impact this industry. The event will also address patent and exclusivity issues, Rx to OTC switches, Good Manufacturing Practices (GMP), advertising and promotion, compliance, enforcement, and related issues.
Susan Lee will speak on the panel, "The New Drug Approval Process: New Drug Research and Development" at FDLI's Introduction to Drug Law and Regulation.
