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?
As a reminder, all discussion posts must be a minimum of 350 words initial, references must be cited in APA format 7th Edition, and must include a minimum of 2 scholarly resources published within the past 5 years.
Important - Read this before proceeding
These instructions reflect a task our writers previously completed for another student. Should you require assistance with the same assignment, please submit your homework details to our writers’ platform. This will ensure you receive an original paper, you can submit as your own. For further guidance, visit our ‘How It Works’ page.