Regulatory Complaint Handling, MDR`s & Recalls - Webinar By GlobalCompliancePanel 2012

  • 01 Aug 2012
  • Webinar

Description

Topics
  • Complaint Documentation
  • FDA`s Complaint Definition 820.3 (b)
  • Part 806 - Reports of Corrections & Removals
  • Part 803 - Medical Device Reporting
  • Complaint Handling Pitfalls
  • Warning letters and other FDA Remedies
Who should Attend
  • Manufacturing & Design Engineers
  • Quality & Regulatory Professionals
  • Corporate & Operations Executives
  • Marketing Product Managers

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Important

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Event Categories

Education: Training
Government & Global Issues: Law & Regulations
Health & Medicine: Healthcare, Hospitals & Clinics, Medical device, Pharma

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