Regulating AI: Is it possible?

Is it possible to regulate AI? If so, how would the U.S. Food and Drug Administration (FDA) do it?

John Sotos, a cardiologist, medical director at Intel and member of the Air National Guard, answers those questions in a guest blog post in the Wall Street Journal.

His take on regulating AI is the FDA cannot test all possible failure scenarios. But, he writes, the FDA can ensure that the system require the physician or radiologist to rate the accuracy of each AI suggestion. Furthermore, each rating would be sent to the FDA, where each AI system would be tallied to show its accuracy. Those ratings would be published online by product name.

Sotos then goes on to discuss the ramifications of such regulation.

Read the rest and make your own judgment:

""

As a senior news writer for TriMed, Subrata covers cardiology, clinical innovation and healthcare business. She has a master’s degree in communication management and 12 years of experience in journalism and public relations.

Around the web

The nuclear imaging isotope shortage of molybdenum-99 may be over now that the sidelined reactor is restarting. ASNC's president says PET and new SPECT technologies helped cardiac imaging labs better weather the storm.

CMS has more than doubled the CCTA payment rate from $175 to $357.13. The move, expected to have a significant impact on the utilization of cardiac CT, received immediate praise from imaging specialists.

The all-in-one Omni Legend PET/CT scanner is now being manufactured in a new production facility in Waukesha, Wisconsin.

Trimed Popup
Trimed Popup