[Webinar] Introduction and overview to ISO 13485 – Why Should You Get Certified?

[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.

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Extending the recognition of CE marking and the implementation of the UKCA mark

Extending the recognition of CE marking and the implementation of the UKCA mark

On the 1st of August, 2023, the UK government announced plans to extend recognition of CE marking ‘indefinitely’ beyond the upcoming December 2024 deadline previously announced.

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