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March 2023

Cybersecurity for Medical Device Manufacturers in EU

Knowledge & Resources /

In December 2022, the European Commission published the new directive (EU) 2022/2555 on measures for a common level of cybersecurity across the Union. This led to the amendment of the regulation (EU) 910/2014 on electronic identification and trust services for electronic transactions in the internal market (also known as eIDAS regulation) and repeals the NIS […]

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Who is EUMEDIQ, anyway? Let’s start the series with: Lisa!

Interview /

In the coming months, we will introduce you to the team. Let’s start with: Lisa! What is your field of expertise? I am mainly responsible for design transfer. I help to ensure that newly developed products also make it to production. My specialty is process development and risk management, making sure all processes run smoothly. I am a safety expert for non-active medical devices and support with sterilization

Who is EUMEDIQ, anyway? Let’s start the series with: Lisa! Read More »