Description
Pharmaceutical regulatory sciences is a multidisciplinary field focused on the development, evaluation, approval, and monitoring of pharmaceutical products to ensure their safety, efficacy, and quality. It plays a vital role in bridging the gap between scientific innovation and public health by guiding how drugs and medical products are researched, manufactured, and brought to market. This field involves understanding and applying regulatory requirements set by agencies such as the U.S. Food and Drug Administration (FDA), the European Medicines Agency (EMA), and other global authorities. Professionals in pharmaceutical regulatory sciences work to ensure compliance with evolving regulations, facilitate the approval of new therapies, and support post-marketing surveillance, all while promoting patient safety and public trust in healthcare products.
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