Wednesday, October 11, 2017 12:16:41 PM
I already know that those results were successful. I'm talking about the next step in the process which are the FDA trials.
It will take 3 months to get approval and then Endonovo can market and sell the device. We then have to report any adverse side effects that come up, if any, from people using the device. Endonovo has to report those to the FDA via the FDA adverse events reporting system. As long as adverse events remain within the range allowed by the FDA, our device continues to be marketed and sold. Because it's non invasive and due to the components used to make e device, the side effects/adverse events will basically be non existent/bare minimal.
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