How to Simplify Your Compliance with the New ISO 13485:2016
Click through for a free webinar from Jon Speer, an 18+ year medical device industry veteran and founder & VP QA/RA at greenlight.guru.
He walked us through all the changes ISO made in its long awaited revision to 13485, the global standard for medical device quality management systems.
This is the first revision of the standard since 2003, and it represents some major changes including the inclusion of risk management throughout the QMS, greater emphasis on quality management throughout the entire product lifecycle and supply chain, and much more.
Specifically you will learn:
• What exactly changed in the new ISO 13485:2016
• How leveraging technology can help simplify your compliance
• 5 steps to take now to make for a smooth transition
• Live Q/A to answer all your questions
BONUS! When you register below, you’ll get immediate access to a QMS Audit Checklist, his past webinar with us, and more.
>> Forward this link to colleagues who would value this content.