EU MDR Archives - Page 2 of 7

EU MDR 6 min read

Turning Complex Medical Data Into Engaging Reader-Friendly Stories

Turning Complex Medical Data into Engaging, Reader-Friendly Stories How to Transform Evidence into Clear, Actionable and Trustworthy Medical Narratives By Dr. Alyssa…

By CiteMed Author

12 Dec 2025

EU MDR 6 min read

EU Clinical Trial Regulation: What you Need to Know

For manufacturers, clinical trials or at least the protocol are already planned and set to go for up to 2023. However, a…

By CiteMed Author

20 Nov 2025

EU MDR Literature Review 12 min read

Meddev 2.7 1 Rev 4: Guidelines for Literature Search

MEDDEV 2.7.1 Rev. 4 remains the most important technical guidance document for conducting literature searches within the European medical device regulatory framework.…

By CiteMed Author

20 Nov 2025

EU MDR 7 min read

ISO Standards for Medical Devices: What they are and When you Need Them

The whole point of medical devices is to improve patient safety and patient quality of life. That's it, that's the gist. To…

By CiteMed Author

20 Nov 2025

EU MDR 6 min read

Self-Certification for CE Mark – An Overview

The gradual implementation of the European Medical Device Regulation (MDR, 2017/745) changed the game for medical device manufacturers commercializing their devices in…

By CiteMed Author

20 Nov 2025