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Webinar
Medical Devices
Active Implantable Medical Devices under the EU MDR at MedTech Summit 2021
This webinar discusses technical documentation requirements under the EU Medical Device Regulation.
In this webinar:
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Active Implantable Medical Devices at BSI.
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Technical documentation requirements under the EU Medical Device Regulation.
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Obstacles for BSI as a Notified Body.
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Evidence to support active implantable medical devices when submitting documents for application.
Active Implantable Medical Devices under the EU MDR at MedTech Summit 2021
Focusing on software design and clinical evidence to support active implantable medical devices when submitting documents for an MDR application.
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Thomas Doerge, Global Head Active Implantable Medical Devices, BSI
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