Blog

PMS and PMCF 5 min read

The Post-Market Surveillance Document: Which Ones Do you Need?

It's not enough to make a device and put it on the market—you must know how people use your product. Therefore, the…

By CiteMed Author

20 Nov 2025

PMS and PMCF 6 min read

PMCF Plan EU MDR: What You Need and How to Create It

One of the new aspects introduced in the European Medical Device Regulation 2017/745 (MDR) is post-market clinical follow-up (PMCF). While PMCF is…

By CiteMed Author

20 Nov 2025

EU MDR 9 min read

Free EU MDR Templates – Download Here

Before you begin (or continue your EU MDR Journey), make sure you're operating off of comprehensive templates. This article will cover a…

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

Literature Review 7 min read

Term Refinement in Literature Search

A literature search is a systematic search through existing data in an organized way to determine an extensive range of quality references…

By CiteMed Author

20 Nov 2025

CER Writing 7 min read

CER Checklist: 12 Attributes of an Excellent CER Writer to meet the Clinical Evaluation Requirements

The European Union Medical Device Regulation (EU MDR) has set higher standards for medical device clinical evaluation ERs) standards. With stricter regulations…

By CiteMed Author

20 Nov 2025

EU MDR 6 min read

The UK MDR and The EU MDR: What Are The Differences?

UK MDR is the primary standard that mandates requirements for anyone selling medical products in the UK, as it is a vast…

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