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Status: Closed

Listing: Private

Created on June 16, 2010 by genomeweb

Ended July 16, 2010

Is the FDA justified in classifiying DTC genetic tests as medical devices?
  • No, they're overreacting to 23andMe's recent lab mixup.
    14%
  • No, they'll limit consumers' access to their own genetic information.
    45%
  • Yes, these tests need to be regulated by FDA.
    27%
  • Yes, and they should restrict access to the tests while they sort it out.
    12%
Created on Jun 16, 2010

Closed

Total Votes: 480

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