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Webinar
Medical Devices
AIMDD to MDR Transition - What You Need to Know
The webinar provides an overview of important topics to be considered when transitioning from the AIMDD to the Medical Device Regulation (MDR).
In this webinar:
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Pre-Submission preparations & considerations.
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MDR Technical documentation review process.
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General feedback on technical documentation.
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Post application activities & responsibilities.
AIMDD to MDR transition - what you need to know
Topics to be considered when transitioning from the Active Implantable Medical Device Directive (AIMDD) to the Medical Device Regulation (MDR).
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Thomas Doerge, Global Head Active Implantable Medical Devices, BSI
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Concetta Gallo, Technical Team Manager, AIMD, BSI
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