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The 2016 revision of ISO 13485 Medical Devices – Quality Management Systems incorporates many changes. In particular, it places a greater focus on risk management than the previous version of ISO 13485.

Medical device manufacturers, suppliers and related parties must understand the changes and how to implement them successfully so they can continue to meet customer needs and comply with regulatory requirements.

Available for online viewing 24/7, our complimentary webinar will help you to ensure a smooth transition to ISO 13485:2016. It provides an overview of the key aspects of the new version of the standard and explains how organizations involved with the medical devices industry will be affected by the changes. Our webinar will show you how we can guide you through the transition.

Agenda

  • Introduction to ISO 13485:2016
  • Structure and Terminology
  • Key Changes to ISO 13485
  • Summary
  • Future Development

Presenter

Magd Hendy – Global Training Manager

Duration

This webinar is 12 minutes in duration.

Target Audience

The webinar is aimed at organizations that need or want to implement ISO 13485:2016.

Language

English

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