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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 In 2017, Congress acted again to update the Common Rule and strengthen the provisions related to consent. These warnings echo those of the U.S.

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Harms and Biases Associated with the Social Determinants of Health Technology Movement

Bill of Health

billion dollars of health system funds were invested into SDOH efforts from 2017 to 2019. Informed Consent and Refusal. Therefore, a proper informed consent and refusal process would involve naming all the ways days could be used throughout the intervention and allowing patients to opt in or out of the individual data use cases.

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Intersectionality, Indigeneity, and Disability Climate Justice in Nepal

Bill of Health

However, severe climate hazards coupled with institutional and structural barriers and limited government responses are challenging their ability to adapt. Additionally, women and girls with disabilities, the deafblind, and persons with psychosocial, intellectual, and other complex disabilities lack effective government support.

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Regulating Medical Assistance in Dying: A Comparison of the U.S. and Canada

Bill of Health

For instance, the 2017 case A.B The federal government did not challenge this decision and instead amended the law in 2021 to expand access to MAID to individuals whose deaths are not reasonably foreseeable. At the time, the law required a person’s natural death to be “reasonably foreseeable” for a person to be eligible for MAID.

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Can Children Consent to the COVID Vaccine? The Case of Foster Care and Juvenile Justice

Bill of Health

Some children may be unvaccinated by no choice of their own, but instead because of decisions made by parents, guardians, or state or local government officials. In this post, I argue that young people should have the opportunity to consent to vaccines. 3] Bell, supra note 99 at 26. [4]

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SQA Regulatory Surveillance Summary | Monthly Update 2023 – January

SQA

To add to these documents, a template for “Substantial modification of performance study under Regulation (EU) 2017/746” is also provided. It includes aspects such as home health visits, remote monitoring and diagnostics, direct-to-patient shipment of study drugs, and electronic informed consent.

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The BFDs – The Ten Best Prescription Drug/Medical Device Decisions of 2023

Drug & Device Law

2023) (federal government may unilaterally obtain dismissal of FCA claims, and calling the constitutionality of the FCA’s private enforcement mechanism into question) ( here ); Quishenberry v. Plaintiff knew about it, too, since he signed an informed consent document mentioning it. Hrymoc was tried in late 2017.

FDA 105