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Regulation: The FDA is overcautious on consumer genomics

Author

Listed:
  • Robert C Green

    (Brigham and Women’s Hospital and Harvard Medical School, and the Partners HealthCare Center for Personalized Genetic Medicine, Boston, Massachusetts.)

  • Nita A Farahany

    (Nita A. Farahany is at the Duke University School of Law and the Duke Institute for Genome Sciences and Policy, Durham, North Carolina.)

Abstract

A US drug-agency clampdown is unwarranted without evidence of harm, say Robert C. Green and Nita A. Farahany.

Suggested Citation

  • Robert C Green & Nita A Farahany, 2014. "Regulation: The FDA is overcautious on consumer genomics," Nature, Nature, vol. 505(7483), pages 286-287, January.
    • Handle: RePEc:nat:nature:v:505:y:2014:i:7483:d:10.1038_505286a
    DOI: 10.1038/505286a
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    Cited by:

    1. Alexander Nill & Gene Laczniak, 2022. "Direct-to-Consumer Genetic Testing and Its Marketing: Emergent Ethical and Public Policy Implications," Journal of Business Ethics, Springer, vol. 175(4), pages 669-688, February.

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