Free Webinar – Planning for FDA Clinical Site Inspections

Join Cato Research for a free educational webinar on Thursday 29 April 2010 at 2PM EST. Cato Research Regulatory Scientist Cathy Anderson will be presenting “Planning for FDA Clinical Site Inspections: Are You at Risk?”

Topics covered will include:

• Responsibilities of FDA, sponsors, and investigators
• FDA site selection: triggers for inspections
• Inspection preparation and management
• High priority items for FDA review
• Outcomes of inspections and recent trends
• Best practices for response to FDA findings

For more information and to register visit: Cato Research Events