Webinar
Medical Devices

MDR Conformity Assessment Routes in the AIMD Space

A SMEs tailored overview of the MDR Conformity Assessment Routes.

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Gaining a better understanding of MDR Conformity Assessment Routes

Presenting an overview of the MDR Conformity Assessment Routes, the application process and BSI approach, tailored to SMEs in the AIMD space.

Discuss classification of devices including accessories.
How to preparing a comprehensive technical documentation package.
Provide general lessons learnt about review timelines and associated service levels at BSI.
Challenges in the CE marking process.

Speakers

Hear from the experts in this webinar

Speaker

Thomas Doerge

Global Head Active Implantable Medical Devices, BSI

Insights & Media

Find out about the latest quality trends with insights from our experts

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EU MDR – Post Market Clinical Follow-Up

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Annex XVI - Devices Without an Intended Medical Purpose

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Using Standards to Demonstrate Conformity

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Unlocking the Potential of Consumer Wearables in Healthcare

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Medical Device Lifetime - Assisting manufacturers

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Symbols & Details Required for Medical Devices & IVDs

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