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Webinar: Implications of the New MDR from a Product Testing and Certification Perspective

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Topic: Implications of the new Medical Device Regulation (MDR) from a product testing and certification perspective

Duration: 45min

Language: English

Content: This webinar will introduce you to the changes of the new Medical Device Regulation (MDR) and how they will impact your Electro-Medical product research, design, and development through to placing your product on the European market. The new regulation will bring about significant changes on clinical, pre-clinical and biocompatibility performance as well as other technical requirements for your business and it’s important to understand the implications early and start planning your transition immediately.

View: Please click this link to view the webinar.

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