In this project, we asked 500 U.S. scientists to share their views on the Direct-to-Consumer testing industry, specifically in the context of the FDA's warning letter to 23andMe, Inc. in November of ...
2013. At that time, the FDA ordered 23andMe to immediately discontinue offering analysis of the genetic data produced by their tests. The FDA was concerned that individuals might make harmful medical decisions based on consumer genetic testing results without the advice of a physician. Our research shows that this was a controversial decision in the minds of scientists.
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