Product Risk Management Under ISO 14971:2007 and ICH Q9 2016

  • 07 Dec 2016
  • Webinar

Description

Product Risk Management Under ISO 14971:2007 and ICH Q9 2016 is a webinar that covers topics such as:

  • ICH Q9 for Pharma
  • The Revised ISO 14971:2007 for Devices
  • Design, Process, and Use[r] Failure Mode, Effects and Criticality Analysis’
  • Product Hazard Analysis
  • The Team and It’s Involvement – Who, When and How
  • Fault Tree Analysis
  • Using the Completed Document – It’s Real Value
  • Product Risk Management File and Report
  • Keeping it "In the Loop"

Product Risk Management Under ISO 14971:2007 and ICH Q9 2016 is intended for attendees from:

  • Internal / External Auditors and/or Consultants
  • Senior Management, Project Leaders
  • Quality Systems Personnel / QAE
  • Regulatory Affairs
  • Product and Process / Manufacturing Engineering Staff
  • New product development, Marketing and R&D
  • Document Control

Past Events

Important

Please, check "Product Risk Management Under ISO 14971:2007 and ICH Q9" official website for possible changes, before making any traveling arrangements

Event Categories

Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Pharma

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