Regulatory Updates

Your essential guide to MDR, IVDR, and EUDAMED compliance in an evolving global landscape

Navigating EU MDR Annex XIV: How to Eliminate Literature Review Bottlenecks in Clinical Evaluations

by HubMed Technologies GmBh, Marketing Hubmed

Introduction The European Medical Device Regulation (EU MDR 2017/745) has fundamentally transformed the regulatory landscape for the MedTech sector. Moving away from the historical pre-market approval...

Clinical Evaluation Report EU MDR MDR Compliance Medea Technical Files

1 Jun 2026

What is EUDAMED and Why is it Critical for Medical Device Manufacturers?

by HubMed Technologies GmBh, Marketing Hubmed

Introduction Digital transformation has fundamentally disrupted the life sciences sector, and regulatory frameworks are evolving rapidly to keep pace. At the center of this compliance revolution sits ...

Clinical Evaluation Report EU MDR EUDAMED MDR (Medical Device Regulation) MDR Compliance Medea Technical Files

25 May 2026