Webinar On - Best Practices in choosing a Regulatory Pathway for your Over-the-Counter (OTC) Drug Product

14 March 2014, Mississauga, Canada

Introduction

Over-the-counter (OTC) drug products are sold directly to consumers without the need of a prescription from a healthcare provider. In the US, these products are regulated by the Food and Drug Administration (FDA). Because of the large number of marketed OTC drug products, FDA reviews the active ingredients and labeling of over 80 therapeutic classes of drugs (e.g., analgesics) instead of individual drug products.