Red Nucleus Training Institute

Providing on-demand training solutions

Drug Development & Approval

~0.50 hrs

This module provides an overview of the pharmaceutical drug development process from discovery through post-marketing surveillance and discusses the regulatory requirements involved in developing, approving, and marketing drugs in the United States, Canada, European Union, Japan, and China.

Module Details

• Recall steps in the drug development process
• Distinguish between clinical trial requirements in the US, EU, Japan, China, and Canada
• Distinguish between marketing approval requirements in the US, EU, Japan, China, and Canada
• Recall the history and growth of managed care
• Identify the different types of managed care plans
• Recognize the varying objectives of stakeholders in healthcare
• Recognize how managed care organizations reduce utilization of healthcare services

Features

• Fully responsive, scrollable e-learning that auto-scales for use on cell phones
• Module-level learning objectives, summary, and self-check questions
• Interspersed interactive learning exercises
• Annual updates
• SCORM compliant

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