Adverse Event Reporting - Best Practices Dietary Supplements 2016

  • 21 Oct 2016
  • Webinar

Description

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

Past Events

Important

Please, check "Adverse Event Reporting - Best Practices Dietary Supplements" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Industry: Food & Beverages

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