curious to see how foundation models will be managed in the context of care delivery.

assuming there would not be "blanket" general approvals for all conditions rather very detailed condition-specific approvals of each clinical finding (pneumonia, pneumothorax..etc.)

top points:
- would be considered a device
- source attribution required / training data / bias / performance
- "human in the loop" requirement
- "opt out" option requirement
- ongoing monitoring required