Emergo by UL consultants are ready to fully support your CE Marking transition from the Medical Devices Directive (MDD) to the MDR.
Let us provide a systematic plan for your company to achieve compliance.
Emergo by UL is an EU Authorized Representative to over 1000 medical device companies.
Our medical device CRO can design and execute your PMCF study in accordance with EU MDR 2017/745 requirements.
Gain an in-depth understanding of the MDR through an on-site training session with one of our expert consultants.
We specialize in reviewing clinical data and can ensure that your report meets European requirements.
Emergo by UL can recommend the most effective path to update your processes.