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How long could a Class III medical device with Class C software take to get FDA approval? For Class III with […]
It is a truth (near) universally acknowledged that software engineers detest creating documentation. And the documentation they do like to generate […]
In his webinar “How to achieve shorter release cycles for medical devices”, Paul Massey (Bluefruit Software’s Founder and Director) talked about […]
UPDATE: This webinar has now happened. We will be releasing content from it in the coming weeks. Medical device software and […]
TIR45 provides guidelines for the development of medical devices using Agile practices. Since publication in 2012, the medical device community has […]