Spotlight on Post Market Surveillance 2017

Spotlight on Post Market Surveillance 2017 is a webinar that covers topics such as:

• FAERS – FDA Adverse Event Reporting System
• Investigating a complaint or MDR
• Best Practices
• Common Mistakes and how to avoid them
• Preparing for an FDA or NB Inspection

Spotlight on Post Market Surveillance 2017 is intended for:

• Individuals participating in Failure Investigations
• Complaint Specialists and Managers
• Regulatory Affairs Personnel
• Individuals analyzing Returned Products/Complaint Analysis
• Clinical Affairs Personnel
• Quality Engineers
• Compliance Specialists
• Complaint Handling Unit Personnel