Pharmaceutical Development and Regulation

Name brands, generics and the FDA

 By the end of this module, viewers will be able to: 

• Describe key steps in the pharmaceutical approval process
• Outline key laws and regulations impacting pharmaceutical development
• Understand the differences between generic and branded drug development
•  Explain patents, exclusivity, and intellectual property

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Additional Helpful Resources for Providers and Teachers:

       PDA formatted version of this module

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      Evaluation tools (sample questions and answers related to the information provided in this module)

      Topical cases for use in small group discussion

      Podcast formatted version of this module

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