The EU MDR has significantly altered the way the healthcare and medical equipment sectors operate in Europe. Compliance standards for medical devices in terms of safety, transparency, and traceability have grown more complex as the earlier Medical Device Directive (MDD) has been substituted by the MDR. For healthcare niches, especially if your speciality includes the production, distribution, or usage of medical devices in the EU, adherence to the MDR compliance is now a regulatory requirement.
This detailed guide explains the fundamental EU MDR Compliance Services for healthcare companies, describes who the regulation pertains to, and gives a useful roadmap for how to prepare for MDR audits. If you work in healthcare or are a healthcare service user, this is a great starting place.
Formally known as Regulation (EU) 2017/745, the EU MDR was totally enacted on May 26, 2021, governing medical device marketing, sale, and usage within the European Economic Area (EEA). Extending application to a broader spectrum of products, improving clinical evaluation criteria, and establishing distinctive device identification (UDI) systems for traceability, the European MDR regulation is a basic deviation from the previous Medical Device Directive (MDD).
