Template Walkthrough: Clinical Evaluation & Post-Market Surveillance

€399
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Everything you need to know for your EU MDR medical device compliance regarding Clinical Evaluation and Post-Market Surveillance. My colleague Sebastian will walk you through our free templates on the MDR Clinical Evaluation and Post-Market Surveillance, and afterwards you'll be able to fill them out for your own company.

What You Will Learn And What's Included

You will get access to 7 videos. After watching them, you should be able to fill out our free templates yourself and achieve compliance with the EU MDR requirements for Clinical Evaluation and Post-Market Surveillance.


Video 1 (05:17 minutes)

  • Understanding the Clinical Evaluation process

Video 2 (06:23 minutes)

  • Understanding the phases of a Clinical Evaluation
  • Writing a Clinical Evaluation Plan

Video 3 (12:36 minutes)

  • Writing a Clinical Evaluation Report

Video 4 (11:51 minutes)

  • Performing a literature research for Clinical Evaluation

Video 5 (06:18 minutes)

  • Performing a database search for Post-Market Surveillance

Video 6 (09:27 minutes)

  • Post-Market Clinical Follow-Up Concepts and Plan

Video 7 (07:51 minutes)

  • Writing a Post-Market Clinical Follow-Up Report


The templates themselves are freely available on our website. If you haven't seen them yet, check them out here:

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If the videos didn't meet your expectations, just send us an email to hello@openregulatory.com to request a refund, no questions asked.

Last updated Jun 3, 2024

You'll get access to 7 videos in which Sebastian walks you through everything you need to know about writing your own Clinical Evaluation and performing your Post-Market Surveillance.

Learn how to create your own Clinical Evaluation
Sebastian will show you how to perform an MDR-compliant clinical evaluation
Learn everything about literature research
Everything you need to know about literature research for MDR compliance.
Learn about Post-Market Surveillance
Understand how to conduct post-market surveillance as part of the EU MDR.
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€399

Template Walkthrough: Clinical Evaluation & Post-Market Surveillance

0 ratings
Buy this