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EU MDR Systematic Review 15 min read

Living Systematic Reviews for Medical Devices: Enabling Continuous Clinical Evaluation Under EU MDR

  Introduction: The Continuous Problem   Under the European Medical Device Regulation (EU MDR 2017/745), clinical evaluation is defined as a continuous process (Article…

By CiteMed Author

29 Mar 2026

EU MDR 11 min read

Navigating Appraisal and Weighting Under MDR 2017/745

  A Comprehensive Guide for Medical Device Evidence Assessment   Introduction   Appraisal and weighting of clinical data are among the most…

By CiteMed Author

17 Mar 2026

EU MDR 13 min read

CER Writing Strategy Guide: How to Write a Compliant EU MDR CER

How to Write a Compliant Clinical Evaluation Report Under EU MDR 2017/745 Introduction The Clinical Evaluation Report (CER) is the central regulatory…

By CiteMed Author

11 Mar 2026

EU MDR 7 min read

In-House vs Outsourced CER Writing Under EU MDR: Strategic Considerations for Medical Device Manufacturers

Introduction Under the European Union Medical Device Regulation (EU MDR), the Clinical Evaluation Report (CER) has become one of the most scrutinised…

By CiteMed Author

03 Mar 2026

Literature Review 13 min read

FDA Literature Review – Class III PMS and Indication Expansion

Introduction Why FDA increasingly expects robust literature evidence for Class III devices For Class III medical devices, the U.S. Food and Drug…

By CiteMed Author

16 Feb 2026

Literature Review 14 min read

Complete Guide to Copyright and Usage for Medical & Literature Review Writers

1. Introduction: Why Copyright Matters in Scientific Writing Copyright is a fundamental yet often misunderstood aspect of scientific writing. Every published research…

By CiteMed Author

07 Feb 2026

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

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