Entering The US Pharmaceutical / Med Device Industry

This comprehensive bundle explores the critical aspects of pharmaceutical regulations, drug development, and federal oversight in the healthcare industry. The courses provide an in-depth understanding of the history and evolution of pharmaceutical regulations, the stages of a drug’s life cycle from discovery to post-market surveillance, the roles of key federal agencies in ensuring drug safety and efficacy, and the FDA’s Office of Prescription Drug Promotion (OPDP) in monitoring prescription drug advertising.