Usability engineering (UE) support for the EU transition to IVDR

We can help your company to plan and document all stages of your UE process, ensuring that your product is safe, effective, and tailored to the needs of users.

European Authorized Representative for Medical Device Companies

Emergo by UL is an EU Authorized Representative to over 1000 medical device companies.

EU IVDR 2017/746 Gap Assessment and CE Transition Support for Medical Device Manufacturers

Let us provide a systematic plan for your company to achieve compliance.

In Vitro Diagnostics Regulation (EU IVDR) Training

Gain an in-depth understanding of the IVDR through an on-site training session with one of our expert consultants.