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The webinar provides an overview of important topics to be considered when transitioning from the AIMDD to the Medical Device Regulation (MDR).
Pre-Submission preparations & considerations.
MDR Technical documentation review process.
General feedback on technical documentation.
Post application activities & responsibilities.
Topics to be considered when transitioning from the Active Implantable Medical Device Directive (AIMDD) to the Medical Device Regulation (MDR).
Reach out and see how we can help guide you on your path to sustainable operational success.