Maximizing Your Certification To ISO 13485

Webinar Type: On Demand

ISO 13485:2016 offers medical device manufacturers a quality management system that translated into greater consistency, improved quality and less risk.

The central principle within the standard, as with other recent updated ISO standards, is risk-based thinking throughout the medical device lifecycle.

With the transition period now complete there are a number of lessons learned, including:

  • How to maintain an effective ISO 13485:2016 QMS after upgrading
  • How to plan and address your internal and external non-conformities

In this webinar, we’ll also review practical examples for the validation of software used in quality management systems and Quality Agreements with suppliers.

Contact Us

Speak to an expert and find out more about how SAI Global Assurance can help you on your way to business excellence.

Speak to an expert to find out more.

Fill in the contact form to receive a callback from our Sales team.

For all other enquiries, please check our FAQs here.
Chat with us