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
- PPYMNTS.com↗Aug 19
- AAuntMinnie↗Aug 19
- TThe ASCO Post↗Aug 21
- NNews-Medical↗Aug 20
- AAmerican Hospital Association↗Aug 18
- MMedical Xpress↗Aug 19