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Learning Objectives

By the end of this module you will be able to:

• Understand drug development from discovery to post-market surveillance
• Be familiar with the role of regulatory bodies in approving drugs for market
• Describe some of the research and regulatory hurdles in drug development

Module Resources

Powerpoint Files

• Drug Development_PPT

SCORM Files

• Drug Development

NOTE: In order to access and adapt the SCORM (Shareable Content Object Reference Model) objects, they must be downloaded and imported into a platform that supports the SCORM standard, for example most common Learning Management Systems.