Regulated Good Practices (GxPs) apply to the development, clinical testing and manufacture of drugs, biological products and medical devices to ensure their safety, efficacy, and security. This employee training course discusses the manner in which regulatory authorities oversee the drug, biologic, and device development and manufacturing processes using GxP regulations. Topics in this eLearning course include: GLPs, GCPs, and GMPs. After completing this module, you will be able to identify what practices comprise the GxP regulations. You will also recognize how these practices relate to each step in the development and manufacture of new drugs, biologics, and medical devices.