Product Risk Management Under ISO 14971 and FDA-ICH Q9 - Webinar By GlobalCompliancePanel 2012

  • 08 Feb 2012
  • Webinar

Description

Topics
  • The Master Validation Plan
  • Verification or Validation -- Recent regulatory expectations
  • When and How to Use DQ, IQ, OQ, PQ
  • Product V&V versus Process / Equipment V&V
  • The 11 Elements of the Software VT&V "Model"
  • Using the Risk Management tools of ISO 14971 and ICH Q9
  • Avoid recent "horror stories" and multimillion dollar fines
Who should Attend

Regulatory Affairs, Senior management, Production, Quality Assurance, All personnel involved in verification and/or validation planning, execution and documentation, Engineering and including Software.

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Important

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Event Categories

Health & Medicine: Healthcare, Medical device, Pharma

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