Taha Kass-Hout will serve in a business development role focusing on healthcare projects. At the FDA, he presided over initiatives at the Office of Informatics and Technology Innovation such as the openFDA program.
The FDA, through its ongoing openFDA project, recently released a new API that will allow users to search for adverse event reports on medical devices going back to 1992. “The API can be a powerful tool for generating hypotheses for further investigation or inquiry and can inform the development of safer, more effective technologies,” Taha […]
Munck Wilson Mandala Partner Greg Howison shared his perspective on some of the legal ramifications around AI, IP, connected devices and the data they generate, in response to emailed questions.
The U.S. Food and Drug Administration has launched a division for health IT entrepreneurs, researchers and interested members of the public to access data on medication errors and drug adverse events using its API, according to a statement by the FDA. The initiative is part of a broader trend as government health administrators see the […]