Are you preparing a 510(k) submission to the FDA? If so, have you identified the correct testing standards for your device? Finding the right testing...
Resource for overview of medical device regs
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A lot of people know that the US Department of Commerce publishes short research reports on the medical device industry in specific countries, but it's worth repeating in case you have not visited in some time. You can read regulatory process overviews on 20+ countries at the Learning Library on our website.