logo

QA/RA Consulting, Auditing & Training

logo

Let's get started

EU MDR TOC

Jan 10, 2024

Table of Contents for the EU MDR 2017/745

group of managers discussing project

Nov 02, 2023

Definitive Guide to Medical Device Clinical Evaluation Reports (CER) and EU MDR Requirements

Sep 30, 2023

EU MDR Equivalence: How Equivalent Does a Medical Device Need to Be According to MEDDEV 2.7/1 rev 4?

Feb 14, 2023

What Is Considered a Significant Change Under EU MDR Article 120(3) and MDCG 2020-3?

Feb 13, 2023

An Overview of Medical Device Periodic Safety Update Reports (PSUR) and Postmarket Surveillance Reports (PMSR) Under the EU MDR

Jan 04, 2023

EU MDR Timeline: Common Questions Answered About the Implementation Extension