Participate in interactive discussions on how to develop drugs and biologics under FDA and ICH Guidelines while proactively overcoming any drug development challenges.


WHAT YOU WILL LEARN
• How the pharmaceutical industry identifies new products and brings them to market
• Contributions of key groups within the company and how they interact
• FDA and regulation of the industry
• The basics of filing a New Drug Application (NDA)
• Ethical considerations in conducting clinical research
• Institutional review, informed consent, and financial disclosure
• Concepts and functions associated with ensuring overall study quality

Event Code:
10430