Introduction to ISO 13485:2016
Learn about key aspects to the implementation of ISO 13485:2016 and impacts to organizations in the medical device industry.
29 Nov 2017, 23:00
30 Jan 2018, 23:00
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
To know more about the ISO 2016:13485 Transition, we have more resources available at this page.
For more information, please contact:
SGS Hong Kong
Tel: (852) 2765 3620
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.