Medical Product Development Part 2: Patent and FDA Issues
In part 2 of this review series on how to engage with the medical device industry as a surgeon, we summarize the patent application process. The federal government must approve any invention you might try to bring to market as safe-to-use for patients before any marketing can be initiated via the Fo...
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Veröffentlicht in: | The Journal of hand surgery (American ed.) 2021-10, Vol.46 (10), p.918-923 |
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container_title | The Journal of hand surgery (American ed.) |
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creator | Nadeem, Maheen Weiss, Arnold-Peter C. |
description | In part 2 of this review series on how to engage with the medical device industry as a surgeon, we summarize the patent application process. The federal government must approve any invention you might try to bring to market as safe-to-use for patients before any marketing can be initiated via the Food and Drug Administration submission process detailed herein. |
doi_str_mv | 10.1016/j.jhsa.2021.07.011 |
format | Article |
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subjects | Development FDA innovation medical products |
title | Medical Product Development Part 2: Patent and FDA Issues |
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