Insights

Filter by Topic
For non-EU manufacturers entering the European market, compliance with EU energy labelling regulations (EPREL/ERP)—notably Regulation (EU) 2017/1369—is essential. This regulation mandates that all energy-related products must be registered in the European Product Registry for Energy Labelling (EPREL) prior to being marketed or sold in the EU.
Adopted on 13 June 2024 and published in the Official Journal of the European Union on 9 July 2024, Regulation (EU) 2024/1860 amends both the Medical Device Regulation (MDR) 2017/745 and the In Vitro Diagnostic Regulation (IVDR) 2017/746. A central change concerns EUDAMED — the European Database on Medical Devices

Contact

Info@Dutchbridgeint.com 

Eprel@Dutchbridgeint.com

Reach Us

Weena 690,
3012 CN Rotterdam

The Netherlands

Dutch Bridge International B.V. 2026