Clinician judgement is a control, not a disclaimer
Diagnosis, exclusion, risk decisions, treatment, prescribing and sign-off remain with appropriately qualified professionals. The interface must make review actionable rather than ceremonial.
Clinician-controlled evidence
Trust and safety
SheldonDx is designed as clinician-supervised workflow and reasoning support. Safety depends on preserving evidence sources, showing uncertainty, requiring review, preventing diagnostic ranking and keeping patient contact and clinical decisions under authorised human control.
Which action would cause harm if a fluent model completed it silently?
Diagnosis, exclusion, risk decisions, treatment, prescribing and sign-off remain with appropriately qualified professionals. The interface must make review actionable rather than ceremonial.
Clinicians should be able to inspect where evidence came from, distinguish observation from inference and see limitations or conflict before accepting generated language.
Pilot status, validation, regulatory classification and performance should be stated narrowly and updated with evidence. A roadmap item must never appear as a shipped control.
Regulatory status depends on intended use, market and released functionality. Request the current product and regulatory statement rather than inferring it from marketing language.
Patient contact must remain within authorised workflows. Autonomous contact is not a general product promise.
Discuss intended use, pilot controls and the evidence your governance team needs.
Email about clinical safety