From the Laboratory to the Marketplace: The Development of a New Drug - Livestream

Drug development requires a delicate balance between innovation, efficacy, safety, and regulatory compliance. This talk will explore the multifaceted process of bringing a new drug from the laboratory to the market, focusing on the critical role of regulatory affairs in ensuring patient safety and product quality. We will examine the key stages of drug development, including pre-clinical studies, clinical trials, and risk-benefit analysis. We will also discuss how to interpret the package insert. We will discuss how drug developers can work with the FDA to bring the new drug to the market.

Speaker: Natalie McClure, St. Mary's University

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