In this enlightening conversation, Anne and Nu Trelle discuss the complexities of over-the-counter (OTC) medications, focusing on the regulations, approval processes, and the importance of compliance with OTC monographs. Nu Trelle shares insights from her extensive experience in the pharmaceutical industry, explaining the differences between OTC and prescription drugs, the significance of labeling for consumer safety, and the stringent requirements for bringing OTC products to market. The discussion also touches on the evolving nature of OTC monographs and the challenges faced by manufacturers in ensuring their products meet safety and efficacy standards.
