EU MDR 2017/745 Gap Assessment and CE Transition Strategy for Medical Device

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

European Authorized Representative for Medical Device Companies

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

European Post-Market Clinical Follow-up Studies (PMCF) for Medical Devices

Our medical device CRO can design and execute your PMCF study in accordance with EU MDR 2017/745 requirements.

On-Site Medical Devices Regulation (EU MDR) Training for Manufacturers

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

MEDDEV 2.7.1 rev 4 and Clinical Evaluation Reports (CER) for Medical Devices

We specialize in reviewing clinical data and can ensure that your report meets European requirements.

EU MDR compliance consulting for cosmetic and aesthetic products

Emergo by UL can recommend the most effective path to update your processes.

Have questions on what Emergo can do for you?

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