Why FPGAs in medical devices are increasingly becoming the focus of software audits and how you can avoid regulatory risks early on. When programmable logic suddenly ends up in a software audit, things can quickly become uncomfortable when the auditor asks you: "Where is your ...
05/14/2026
Many medical technology companies face the central challenge of transferring a developed medical device from development to series production – while complying with MDR, ISO 13485, and achieving full audit readiness. This is particularly true for prototype production, small-batch production, and early series production. ...
04/16/2026
Regional, traceable, resilient: Why MedTech is reinventing its supply chains. How geopolitical risks, dependence on China, and stricter regulations are fundamentally changing production and supply chain strategies in medical technology. Global MedTech supply chain at its limit. Imagine a medical technology company that previously faced ...
03/19/2026
In wireless distributed systems, each node runs its own hardware clock. Even identical embedded systems start with different time values, run at slightly different frequencies, and experience variable delays when sending, receiving, and processing data. Without synchronization, a ...
According to the German Resuscitation Registry 2024, 370 people per day in Germany suffer a sudden cardiac arrest. That's over 136,000 cases per year, mostly outside of hospitals [1]. The good news: More and more people are intervening. ...
01/20/2026
We are delighted to announce the further strengthening of our team at MEDtech Ingenieur: Since January 15, 2026, Lea Schöppach has been supporting us in the areas of quality management, testing, and production engineering. With her solid training in medical technology and her enthusiasm for quality and technical precision, she brings valuable expertise to the team. ...
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