What is GxP, and what are its regulatory requirements? ddregpharma.wixsite.com
GxP refers to guidelines and regulations that ensure the quality and safety of pharmaceutical products, medical devices, and food products. GxP is an umbrella term that includes Good Manufacturing Practice (GMP), Good Laboratory Practice (GLP), Good Clinical Practice (GCP), and other related regulations. These regulations are enforced by various regulatory agencies worldwide, including the US Food and Drug Administration (FDA) and the European Medicines Agency (EMA). Read our latest blog, “What is GxP,” to learn more.
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