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Exploring the increasing global concerns over the effect of Per- and polyfluorinated alkyl substances (PFAS) on the environment and human health.
This insightful webinar will be beneficial to all BSI Medical Devices clients and manufacturers.
The timeline and steps of the restrictions to production and use of PFAS in medical devices.
What the next steps may be for manufacturers and how best to engage with the Notified Body.
Main challenges that medical device manufacturers are expected to face in the near future.
The impact the challenges will have on CE marking of manufacturers medical devices.
Head of UK Approved Body, BSI
Principal Technical Specialist & Scheme Manager, BSI
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