Articles - Citemed

CER Writing 8 min read

So you’ve taken a look at EU MDR transitions for some of your devices and shopped around for quotes on help writing…

By CiteMed Author

20 Nov 2025

EU MDR 7 min read

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

CER Writing 12 min read

Thinking of Hiring a Clinical Evaluation Consultant? So it's finally time to either start that new Clinical Evaluation Report (CER) project for…

By CiteMed Author

20 Nov 2025

Literature Review 7 min read

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

PMS and PMCF 6 min read

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 5 min read

The MDR is a sweeping reform of medical device regulation in Europe that aims to strengthen safety and quality. Recently, the provisions…

By CiteMed Author

20 Nov 2025

IVDR 6 min read

CE marking indicates compliance with an EU directive so that you can market your products in the EU. It's that simple. CE…

By CiteMed Author

20 Nov 2025

CER Writing 6 min read

The medical device industry has been changing bit by bit every day, and one of the significant changes is the addition of…

By CiteMed Author

20 Nov 2025

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