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The Dr. Oz Paradox

Bill of Health

Professionals within a professional relationship are subject to a variety of legal constraints, such as informed consent requirements or professional malpractice liability if things go wrong. What happens if he continues to give bad health advice in what is then a government role? Dr. Mehmet Oz (@DrOz) April 3, 2020.

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The Legal and Ethical Imperative of Explicit Consent in Intimate Medical Procedures

AIHC

However, sensitive exams and other intimate tasks conducted without consent can leave patients feeling violated. Informed consent is a cornerstone of ethical medical practice. of them expressed a correct understanding of what constitutes informed consent. [3] Written by: Shelby Harriel-Hidlebaugh, M.Ed.

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Actionable Insights from the International Collaborative Research Program in Bioscience Innovation & Law

Bill of Health

Emma Kondrup looks at how AI-driven medicine may change how we understand informed consent, and whether existing legislative frameworks provide a good enough safeguard against its risks. Can current EU rules appropriately respond to potential privacy risks and efficacy concerns without unduly hindering innovation?

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Understanding Whistleblower Protections in Healthcare – Legal Obligations and Compliance Implications

AIHC

Atkins, PhD, MSW, LMSW, CPC, CIGE The governments new whistleblower complaint portal launched in April 2025 emphasizes the importance of complying with regulations related to qui tam suits, OCR investigations and protecting the rights of employees submitting a tip or complaint internally or to authorities. Written by Dr. Stacey R.

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Governing Health Data for Research, Development, and Innovation: The Missteps of the European Health Data Space Proposal

Bill of Health

By Enrique Santamaría Together with the Data Governance Act (DGA) and the General Data Protection Regulation (GDPR), the proposal for a Regulation on the European Health Data Space (EHDS) will most likely form the new regulatory and governance framework for the use of health data in the European Union.

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AI’s Ability to Manipulate Decision Making Requires a Moratorium on Its Use in Obtaining Consent for Biomedical Research

Bill of Health

The federal government’s commitment to assuring that participants in human subject research provide fully informed consent dates back to the U.S The World Health Organization supports this ban and in particular describes it as making informed consent impossible in the health care setting.

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New Evidence on Dementia, Identity, and Decision-Making

Bill of Health

In contrast, if participants concluded that Robin was no longer, in the ethically meaningful sense, the person she had been previously, participants might think we must move beyond our default posture of recognizing personal decision-making, to some other system, perhaps governed by pre-existing advance directives.

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