When requirements start to become fragmented... The larger and more complex a medical device development project becomes, the more information is generated. Requirements are documented in documents, technical decisions are recorded elsewhere, and tests are documented in separate files. ...
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 ...
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 ...
02/05/2026
What difference can a CPR feedback system make to cardiopulmonary resuscitation? In the event of cardiac arrest, the transport of oxygen to the body's cells stops immediately, leading to irreversible damage. Cell death begins after just three minutes. This process ...
Usability is generally highly valued – yet it is still often neglected. Why is that? Because usability often only becomes noticeable when it's missing. It's difficult to measure, isn't always specified – and in ...
In previous blog posts, I introduced two essential components of a simple and universally applicable software architecture: events with dispatchers, listeners, and a data pool. This already allows for the easy implementation of many simple use cases. But it's only simple in... ...
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