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Dr. Oliver Eidel bei der Digital Medicine Week 2021 vom health innovation hub (hih)

Dr. Oliver Eidel · Clinical Evaluation · Published March 04, 2021

Oliver ist Arzt, Software-Entwickler und Berater und erzählt ein paar Geschichten aus Healthcare-Startups, die Medizinprodukte konform entwickeln wollten. Anschließend überlegt er, wie man regulatorische Compliance mit OpenRegulatory weniger schmerzhaft gestalten kann. Zum Schluss gibt er den Zuschauern noch drei schnelle Tipps von Mutti.

Der Vortrag war Teil der Digital Medicine Week (DMW) 2021, einer (virtuellen) Konferenz vom health innovation hub (HIH).

Weitere Informationen zur Digital Medicine Week: https://dmw.hih-2025.de
OpenRegulatory-Webseite: https://www.openregulatory.com

0:00 Vorstellung durch Jan Brönneke
1:12 Warum bin ich hier?
5:52 Zwei echte Geschichten aus Startups
12:06 Wie können wir Compliance weniger schmerzhaft gestalten?
17:58 OpenRegulatory Templates und Community
19:55 Drei schnelle Tipps von Mutti
23:41 Tschüß

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How can the usability of the MDR and related standards be improved for startups?

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One user described difficulties in applying the Medical Device Regulation (MDR) and related standards, especially as a startup. The user finds the regulations and standards difficult to read and under

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Great question! I think improving the usability of the MDR and related standards is a big challenge, especially for startups. The MDR is law and ISO s

How is medical device regulation developed and how can its usability be improved for start-ups?

Anonymous · 1 comment

I am interested in understanding how medical device regulation, specifically the MDR, is developed and what could be done to improve its usability, especially for small start-ups. From my experience a

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Regulation like the MDR is developed at the EU level as part of the "new legislative framework" for product safety. The process involves EU institutio

Dr. Oliver Eidel

Dr. Oliver Eidel

I’m a medical doctor, software engineer and regulatory dude. I’m also the founder of OpenRegulatory.

Through OpenRegulatory, I’ve helped 100+ companies with their medical device compliance. While it’s also my job that we stay profitable, I try to dedicate a lot of my time towards writing free content like our articles and templates. Maybe that will make consulting unnecessary some day? :)

If you’re still lost and have further questions, reach out any time!

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