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The continued evolution of mobile devices for medical care expanded use of clinical decision support, and the emergence of machine learning algorithms in medical care have led to the FDA setting standards for these functions. Does the FDA regulate mobile devices, such as smartphones or tablets, and mobile app stores?
If they DO regulate them– is that benefiting the public? Why or why not?
If they DON’T regulate them– should they? Why or why not?
Post must be a minimum of 350 words not including references, references must be cited in APA format 7th Edition, and must include a minimum of 2 scholarly resources published within the past 5 years
REFERENCES Must have DOI Numbers for professor to look them up
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