Europe

Blog

Effect of MDR Implementation on Clinical Trial Submissions

Maaike Labots
Manager, Medical Writing

Fact Sheet

Streamline Your EU MDR Compliance With Avania

Blog

Medical Device Regulation in the UK

May 3, 2024

Blog

Navigating Notified Body Feedback for Clinical Evaluations: The 5 Most Common CER Flaws & How to Avoid Them

April 26, 2024

White Paper

Guidance on Exemptions From The Requirement to Perform Clinical Investigations Pursuant to Article 61(4)-(6) MDR

Blog

A Brief Guide: How the MHRA Regulates Healthcare Software and AI in the UK

April 3, 2024

White Paper

Post-Market Clinical Follow-Up (PMCF): Best Practices for Success

Blog

Clinical Evaluations From MDD to MDR

May 11, 2022

Blog

EU Medical Device Regulation 2017/745 – First Formal Amendment, Delaying Date of Application

May 4, 2020

Blog

Medical apps under the new European MDR

April 6, 2020

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