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EU MDR 11 min read

Literature Reviews for EU MDR

Want to know what the most commonly criticized document in an MDR submission is? Your clinical literature review. Reviewing the literature is…

By CiteMed Author

20 Nov 2025

EU MDR IVDR 6 min read

How Literature Review Automation Improves Performance Evaluation Reports (PER) Program Management for the IVDR

A literature review is a formal collection of scientific studies published in peer-reviewed journals or conference proceedings that are relevant to the…

By CiteMed Author

20 Nov 2025

EU MDR 7 min read

Effectively Handling Corrective and Preventive Actions (CAPA) Process with EU MDR

The EU MDR emphasizes field safety corrective actions to correct non-conformances of the distributed product, but since these principles are used throughout…

By CiteMed Author

20 Nov 2025

Systematic Review 18 min read

Choosing the Best Systematic Literature Review Tools

We have performed 100s of literature reviews over the last few years across medical device and pharma, and here’s what we’ve found.…

By CiteMed Author

20 Nov 2025

Systematic Review 4 min read

Lesson 3 – Systematic Literature Review Course: Literature Search Terms and PICO

Missed last week? Read our Past Lesson: Selecting Your S&P Criteria and Clinical Claims. Be sure to check it out if you…

By CiteMed Author

20 Nov 2025

EU MDR 8 min read

Breaking Down EU MDR Implementation for Class 1 Medical Devices

Breaking Down EU MDR Implementation for Class 1 Medical Devices Following the one-year delay in the MDR Date of Application, the Class…

By CiteMed Author

20 Nov 2025

PMS and PMCF 9 min read

Post Market Surveillance EU MDR – CiteMed

Post-market surveillance (PMS) under the EU MDR (2017/745) is a systematic and proactive process through which medical device manufacturers collect, analyze, and…

By CiteMed Author

20 Nov 2025

EU MDR 10 min read

Performing Effective Literature Search – For EU MDR and Other Regions

For any medical device, there must be sufficient clinical evidence to corroborate compliance with relevant essential requirements for safety and performance. One…

By CiteMed Author

20 Nov 2025