Should We Regulate Direct-to-Consumer Health Apps?
Over 318,000 health apps are available in app stores, but only a fraction are regulated by the U.S. Food and Drug Administration.

Over 318,000 health apps are available in app stores, but only a fraction are regulated by the U.S. Food and Drug Administration.
This post originally appeared in Device and Materials Engineering. You can read it here. By Sara Gerke & I. Glenn Cohen In our new paper, we discuss the ethical challenges of ingestible electronics sensors (IESs; also called “smart pills”) and examine the legal regulation of such sensors in the United States and Europe. IESs are…
A recent US lawsuit highlights crucial challenges at the interface of data utility, patient privacy & data misuse By Timo Minssen (CeBIL, UCPH), Sara Gerke & Carmel Shachar Earlier, we discussed the new suit filed against Google, the University of Chicago (UC), and UChicago Medicine, focusing on the disclosure of patient data from UC to…
By Timo Minssen (CeBIL, UCPH), Sara Gerke & Carmel Shachar A recent US lawsuit highlights crucial challenges at the interface of data utility, patient privacy & data misuse The huge prospects of artificial intelligence and machine learning (ML), as well as the increasing trend toward public-private partnerships in biomedical innovation, stress the importance of an effective…
A new working paper from participants in the AI-Health Working Group sets forth a research agenda for stakeholders to proactively collaborate and design AI technologies that work with users to improve their health and wellbeing.
If you ask someone to define AI, you will get no universal answer. One of the key challenges in legislating AI will be to define it.