Event Date/Time: Dec 08, 2010
Report as Spam

Description

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

Venue

800 Enterprise Rd Ste 200,
Horsham
Pennsylvania
United States
MORE INFO ON THIS VENUE