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EU MDR 10 min read

Why Mendeley and Citation Managers Are Not Enough for EU MDR Literature Review

Mendeley and Reference Management Software: Why They Fall Short for EU MDR Clinical Evaluation Introduction The use of reference management software and…

By CiteMed Author

03 Jun 2026

Literature Review 10 min read

How Long Does a Medical Device Literature Review Take Under EU MDR?

Medical Device Literature Review Timelines: What Really Determines How Long It Takes As regulatory expectations continue to evolve, literature review has become…

By CiteMed Author

29 May 2026

CER Writing EU MDR 10 min read

CER Checklist for EU MDR: A Practical Framework for Clinical Evaluation Report Pre-Submission Review

EU MDR CER Checklist: What to Review Before Submitting Your Clinical Evaluation Report Clinical Evaluation Reports are central to demonstrating the safety…

By CiteMed Author

19 May 2026

Literature Review 13 min read

CiteMed vs Covidence: Choosing the Right Literature Review Software for Medical Device Regulation

CiteMed vs Covidence: Which Literature Review Tool Is Right for Regulatory Use? Covidence and CiteMed's Evidence Cloud are both widely used tools…

By CiteMed Author

16 May 2026

Literature Review 13 min read

CiteMed vs DistillerSR: Choosing the Right Medical Device Literature Review Software

CiteMed vs DistillerSR: Which Approach to Medical Device Literature Review Is Right for You? Introduction At first glance, platforms such as DistillerSR…

By CiteMed Author

16 May 2026

EU MDR 12 min read

CER Rejection: Common Reasons Clinical Evaluation Reports Fail EU MDR Review

Why Clinical Evaluation Reports Are Rejected Under EU MDR - and How to Avoid It Introduction Clinical Evaluation Reports (CERs) play a…

By CiteMed Author

12 May 2026

CER Writing 15 min read

CER Writing: Common Literature Review Challenges Affecting Clinical Evaluation Reports

CER Writing and Literature Review: Common Challenges Affecting Clinical Evaluation Reports Under EU MDR Literature review forms a central component in clinical…

By CiteMed Author

05 May 2026

EU MDR 10 min read

EU MDR Clinical Evaluation Consultant Selection Guide

EU MDR Consultant Selection: What Matters Most   Selecting the right EU MDR consultant is often more challenging than expected. Many manufacturers…

By CiteMed Author

21 Apr 2026

EU MDR 11 min read

FDA’s RWE Guidance Updates: What Manufacturers Need to Know

Introduction In early 2026, the U.S. Food and Drug Administration (FDA) signaled a meaningful shift in how real-world evidence (RWE) can be…

By CiteMed Author

15 Apr 2026