We’d Love to Hear From You!
This website is the result of a personal journey through the intricate world of MR medical device trial compliance in Switzerland and the EU. Built entirely by one researcher who navigated the legal and regulatory landscape by learning through doing, it aims to share practical insights, templates, and real-world examples that can help others on similar paths.
Because of this hands-on origin, we are especially eager to receive your feedback—be it positive encouragement, constructive criticism, or corrections of any inaccuracies you might find. If you notice errors, outdated information, or missing aspects that could be valuable to fellow researchers, please don’t hesitate to let us know.
Quick feedback? At the bottom of every page there’s a comment box—scroll to the Comments section to add your remarks and suggestions.
We are also very keen to learn from the experiences of other MR scientists and study teams working under the Swiss ClinO-MD, MedDO, EU-MDR, or similar frameworks. Your stories, tips, and even your frustrations can help enrich this resource and build a more supportive community for MR research compliance.
Thank you for taking the time to visit this site and for considering reaching out. We look forward to hearing from you!