Food and drug administration’s regulatory shift on direct-to-consumer genetic tests for cancer risk

Author:

Yang Y. Tony123ORCID,Zettler Patricia J.4

Affiliation:

1. Center for Health Policy and Media Engagement, School of Nursing; George Washington University; Washington DC

2. Department of Health Policy and Management; Milken Institute School of Public Health, George Washington University; Washington DC

3. George Washington University Cancer Center; Washington DC

4. Center for Law, Health & Society; Georgia State University College of Law; Atlanta Georgia

Publisher

Wiley

Subject

Cancer Research,Oncology

Reference11 articles.

1. US Food and Drug Administration FDA authorizes, with special controls, direct-to-consumer test that reports three mutations in the BRCA breast cancer genes https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm599560.htm 2018

2. Kalorama Information The market for direct-to-consumer genetic health testing https://www.kaloramainformation.com/Direct-Consumer-Genetic-Health-Testing-11370673/ 2018

3. US Food and Drug Administration 23andMe, Inc https://www.fda.gov/ICECI/EnforcementActions/WarningLetters/ucm376296.htm 2013

4. US Food and Drug Administration De novo classification process https://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/ucm080197.pdf 2017

5. The risk of cancer associated with specific mutations of BRCA1 and BRCA2 among Ashkenazi Jews;Struewing;N Engl J Med,1997

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