Posted: March 10th, 2016
What is the approval process to bring a medical device to market in the US?
1. What is the approval process to bring a medical device to market in the US?
2. Who should be held responsible for detrimental health effects related to that medical device or product? ….What if the device or product were being used in an “off-label” manner, or not in accordance with manufacturer’s directions?
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