Proper Documentation of Risk Management for Compliance with ISO 14971 - Webinar By GlobalCompliancePanel 2012

  • 08 May 2012
  • Webinar

Description

ISO 14971 is an ISO standard that represents the requirements for a risk management system for medical devices.

Proper Documentation of Risk Management for Compliance with ISO 14971 is a webinar that covers topics such as:

  • Choosing the right risk management tools
  • Exploring the Risk Management tool set
  • Meeting Human Factors regulatory requirements
  • What tools are used during each phase of design?
  • How to develop an FMEA that meets requirements
  • How to document standards compliance

Proper Documentation of Risk Management for Compliance with ISO 14971 brings together Design Engineers, Product Risk Management, Medical/Clinical Project Team members, Human Factors Engineers, Process Engineers, Project Managers and Quality Engineers.

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Important

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Event Categories

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

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