ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements 2014

  • 30 Oct 2014
  • Webinar

Description

Topics
  • How ISO 1497:2012 differs from ISO 14971:2007
  • What is ISO 14971
  • How to make sure your Risk Management procedure assures you can meet your CE mark requirements for Risk Analysis
  • How to update your Risk Analysis to meet continued compliance to the European Medical Device Directive(MDD)
Who should Attend
  • Regulatory Affairs
  • Quality Management
  • Design Engineers
  • Quality Engineers
  • Quality auditors
  • Compliance managers

Past Events

Important

Please, check "ISO 14971:2012 - Does your current Risk Analysis still comply with your CE Mark requirements" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Quality assurance
Government & Global Issues: Law & Regulations
Health & Medicine: Medical device

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