Vokinger KN, Feuerriegel S, Kesselheim AS - Lancet Digital Health
The authors discuss the regulatory challenges of AI/ML medical devices capable of continual learning, noting that no such adaptive device has yet been FDA-approved. Known risks, including dataset shift, bias, and catastrophic forgetting, require novel regulatory frameworks.
VIEW SOURCE
Daval CJR, Kesselheim AS - STAT
Mulsant SS, Kesselheim AS, Naci H - Journal of Cancer Policy
Jaiswal N, Gorijavolu R, Thomas S, Hwang TJ, Celi LA, Kesselheim AS - Food and Drug Administration (FDA)