In 2017, the European Union adopted new regulations to improve transparency to information relating to medical devices. But do these laws go far enough to protect patient safety and improve public health?
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By: Angela Gamalski.
As medical device technology expands, so does the need for regulation to assure that patients are protected from malfunctioning devices. South Africa expanded its medical device regulation, modeled on the EU’s medical device directive, just prior to the 2017 Medical Device Regulation. What does this mean for South African technology innovators?
Image credit: https://commons.wikimedia.org/wiki/File:Manual-external-defibrillator-monitor.jpg
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