FDA seeks feedback on potential regulatory approaches for generative AI-enabled medical devices
The FDA is soliciting public input on new regulatory frameworks for medical devices that integrate generative AI. This initiative explores implementing clinician-style performance testing to ensure these technologies remain safe and effective when assisting in patient care or diagnostic decisions.
Covered by 6 sources
- TThe ASCO Post↗18h ago
- NNews-Medical↗2d ago
- AAmerican Hospital Association↗3d ago
- PPYMNTS.com↗2d ago
- AAuntMinnie↗2d ago
- MMedical Xpress↗2d ago