Clinician-researchers deeply invested in data gathering are still obliged to respect a patient-subject’s right to stop being in research.

Improving candidate evaluation and informed consent is key to motivating authenticity, not just voluntariness.

Clinical applications of AI prompt consideration of how responsibility should be distributed among professionals, tech companies, and others.

Transplant physicians must respect indecisive patients’ autonomy while continuing to educate them during their progress towards transplantation.

More transparent pricing would allow patients and families to make better decisions, but there are limitations to how reliably it promotes efficiency and market discipline.

What are insurance, contract, and criminal law implications of detecting Alzheimer’s disease early?

Dr Christy Cauley joins Ethics Talk to discuss her article, coauthored with Dr Zara Cooper: "Which Priorities Should Guide Palliative Surgical Research?"

Heightened caution, improved physician and patient communication, and equitable access are key priorities.

Device innovation has potential to improve patient outcomes over time, yet prospective benefits must be considered in light of risks.

Information different patients need or want about cybersecurity risk varies, so communicating clearly is always key.