Sunday, September 7, 2014

Software Development for Medical Devices

Until recently, safety regulations for medical device software, at least formally, were not exceptionally rigorous across the board. In addition, software was not formally classified as a medical product by the Medical Devices Directive. This has now changed. A new regime is in force governing all medical device software development for all classes of device.
Very good article on software development of medical devices click here to read.



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