Medical Devices
and Software

VDE MeSo offers hands-on support for the approval and certification of medical devices and software.
Get your product to market faster.


Take advantage of the MeSo community to learn about the latest news and discuss it with other experts.

MeSo 2020

The experts community for medical devices and software will meet in Frankfurt. Be on board.


Find articles on medical device regulation and understand how to get your product to market faster.

98000 Words in MDR (EU) 2017/745
196.17287037037 Days until MDR application
> 200 Medical Device Standards
10 + XEC Guidances and Specifications

What our partners say

About our range of services

Thorsten Prinz

"Regulatory of medical devices is a real hurdle, especially for small and medium-sized companies. Practical support from VDE MeSo ensures your success."

Hans Christian Wenner

"Innovative medical devices need up-to-date approaches to satisfy current and future regulatory requirements."

Andreas Rösch

"In a constantly changing environment, VDE MeSo helps to plan and implement sophisticated medical device projects.”

Christian Schübel

"VDE MeSo offers most reliable and current information accelerating market access.”

627 FDA Software Recalls (2011-2015)
> 400 CFR 21 Parts
> 300 Recognised Consensus Standards
712 FDA Medical Device Guidances

Get in touch

To arrange a consultation or workshop, send us a message or give us a phone call: +49 69 6308 349

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