[Webinar] Introduction and overview to ISO 13485 – Why Should You Get Certified?
Join the Eurofins E&E medical device team from the UK on the 6th December 2022 for our latest webinar where we'll cover ISO 13485, the internationally recognised standard for quality management systems specifically within the medical device industry.
Patient safety is paramount in the highly regulated world of medical devices, and product quality is non-negotiable. ISO 13485 is the internationally recognised standard for quality management systems, specifically within the medical device industry.
Organisations certified to ISO 13485 can demonstrate their ability to provide medical devices, or related parts and services, that consistently meet market demands and applicable regulatory requirements.
We will provide an overview of the latest version of ISO 13485 and discuss how it fits into the overall family of quality standards, the associated directives and regulations, and how Eurofins can help you with your medical device certification needs.
If you’re new to ISO 13485, this is the ideal opportunity to understand how this standard can be applied. If you’re already certified to ISO 13485, why not use this as an opportunity to ask questions of our team or update your knowledge?
What’s on the agenda?
In the webinar our Senior Medical Device Auditor, Mark Masnyj, will cover:
- Background and evolution of the ISO 13485 standard
- Who is ISO 13485 for?
- Overview and structure of ISO 13485:2016
- Why get ISO 13485 certified?
At the end of the webinar, we will have a Q&A session to cover any questions around any of the aspects covered and we will introduce the range of medical device certification services, including ISO 13485, available from Eurofins E&E UK.
Register now here to reserve your place.