Take a look at our infographic detailing the key regulatory processes for medical devices that incorporate nanomaterials under the EU Medical Device Regulation (MDR).
In this resource, we explore how to approach the classification, evaluation, and documentation required to ensure compliance. As nanotechnology becomes increasingly integrated into medical devices, it’s essential to understand the unique challenges and regulatory expectations involved.
Our infographic provides a clear and structured overview to help manufacturers, regulatory professionals, and innovators confidently navigate these requirements.
View the full infographic for a comprehensive guide to EU compliance for nanomaterial-based medical devices.
If you require any further information, contact us at: [email protected]
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