Adverse Event Reporting - Best Practices Dietary Supplements 2016

Key Topics

• Personnel training
• Adverse Event Complaints responsibility
• Assessing Adverse Event Complaints
• Receiving & recording Adverse Event Complaints
• Reviewing Adverse Event Complaints
• Adverse Event Complaints records system
• Product withdrawal or recall
• Adverse Event Complaints assessment

Who should Attend

• Regulatory affairs professionals
• Regulatory Affairs managers, directors & Associates, Product safety managers, Compliance Specialist
• Dietary supplement manufacturers, marketers
• Senior management executives (CEO, COO, CFO, etc)
• Legal and medical experts involved in dietary supplements industry
• Regulatory compliance associates and managers
• People investing in FDA-regulated product development projects