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Learn about key aspects to the implementation of ISO 13485:2016 and impacts to organizations in the medical device industry.

Starts

24 Feb 2017, 09:30

Ends

25 Feb 2017, 17:30

Location

Hong Kong, China

ISO 13485


Has your organization’s medical devices already met regulatory requirements?

The ISO 13485:2016 standard was published in February 2016. Registered organizations have a 3-year transition timeline in which to transition their management systems to meet the new requirements. View our on-demand webinar to know more about the latest revision.

In this 12-minute webinar, you will learn:

  • Overview of key changes and developments for ISO 13485:2016, including changes to quality management systems
  • Structure and terminology for the new ISO 13485 update
  • Next steps for getting certified to ISO 13485:2016

For more information, please contact:

SGS Hong Kong
Tel: (852) 2765 3620
Email: hk.cbe@sgs.com  


About SGS
SGS is the world’s leading inspection, verification, testing and certification company. SGS is recognized as the global benchmark for quality and integrity. With more than 85,000 employees, SGS operates a network of over 1,800 offices and laboratories around the world.