Understanding ISO 13485-FDA Requirements for Medical Devices 2015

  • 18 Aug 2015
  • Webinar

Description

Understanding ISO 13485-FDA Requirements for Medical Devices 2015 is a webinar that covers topics such as:

  • Which areas are being revamped under ISO 13485: 2015?
  • What is in store for currently marketed medical devices when ISO 13485: 2015 gets launched?
  • What sort of gap analysis is a must?
  • Where does one begin?
  • When is your quality system expected to be completely switched over to cater to the changes being introduced?

Understanding ISO 13485-FDA Requirements for Medical Devices 2015 is intended for:

  • Quality Assurance
  • Quality and Regulatory Managers
  • ISO 13485: 2015, Medical device regulations, Quality system for medical devices
  • Supplier Management and auditing professionals in the medical device or medical device-pharmaceutical industry quality professionals all across the world

Past Events

Important

Please, check "Understanding ISO 13485-FDA Requirements for Medical Devices" official website for possible changes, before making any traveling arrangements

Event Categories

Business: Quality assurance
Education: Training
Government & Global Issues: Law & Regulations
Health & Medicine: Medical technology

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