MedTech Compliance Articles

Expert guides on EU MDR, Clinical Evaluation, and Literature Review strategies.

CiteMed | EU MDR & Clinical Evaluation Insights

In-depth articles and resources on EU MDR, IVDR, and clinical evaluation for regulatory affairs professionals.

By CiteMed Author|2026-07-03T06:09:36+00:00March 3rd, 2026|EU MDR|

By CiteMed Author|2026-06-02T19:32:29+00:00November 20th, 2025|EU MDR|

Breaking Down EU MDR Implementation for Class 1 Medical [...]

By CiteMed Author|2026-07-03T09:30:10+00:00November 20th, 2025|PMS and PMCF|

Post-market surveillance (PMS) under the EU MDR (2017/745) is [...]

By The CiteMed Team|2026-06-04T20:43:57+00:00November 20th, 2025|EU MDR|

For any medical device, there must be sufficient clinical [...]

By The CiteMed Team|2026-07-03T12:16:33+00:00November 20th, 2025|Systematic Review|

Welcome to the Systematic Literature Review Course! We’re thrilled [...]

By CiteMed Author|2026-07-20T10:06:11+00:00November 20th, 2025|Systematic Review|

We have performed 100s of literature reviews over the [...]

By CiteMed Author|2026-07-03T12:18:34+00:00November 20th, 2025|Literature Review|

Who This Was Written For? To celebrate the latest [...]

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