The U.S. Food and Drug Administration (FDA) is requesting your input on patient safety, including best practices to promote patient safety, education, and competency, associated with the medical software functions excluded from the device definition by the Cures Act for inclusion in a report to the public. Software functions excluded from the device definition include:
- administrative support for health care facilities
- encouragement of healthy lifestyles
- electronic patient records
- transferring, storing converting formats, or displaying data
- providing limited clinical decision support
No hay comentarios:
Publicar un comentario