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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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When the Promises of a Policy Do Not Meet the Reality of Its Practice: Ethical Issues Within Oregon’s Measure 109

Bill of Health

What about informed consent and other ethical issues? While the current informed consent form used by facilitators does address some aspects of concern ( like the use of touch , 333-333-5040 (9) ), it does not address other aspects like suggestibility or power dynamics within the facilitator/client relationship.

Licensing 111
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Managing Healthcare Compliance in Colorado

MedTrainer

This article provides an overview of key factors you’ll want to know about healthcare compliance in Washington. These agencies help maintain the integrity and quality of healthcare services in Colorado, protecting the public and promoting patient safety.

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Introduction to Telebehavioral Health

AIHC

This article is not intended as legal or consulting advice. If your practice is currently using a telebehavioral health approach for patient treatment, or if you organization is considering implementing this approach, we hope this article will give some food-for-thought on the topic.

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

Bill of Health

This article addresses key harms and biases associated with the SDOH technology movement, and provides suggestions to address these issues going forward. Informed Consent and Refusal. Ultimately, SDOH implementers, evaluators, and stakeholders should: Establish mechanisms for informed consent and refusal.

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SQA Regulatory Surveillance Summary | Monthly Update 2023 – January

SQA

The application/notification must be submitted via the EUDAMED database (Article 69 IVDR). ICMRA recognizes that AMR is a complex, multifaceted problem and calls for better coordination across all sectors, including public health, animal health, and the environment, through a ‘One Health’ approach.

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SQA Regulatory Surveillance Summary 3 | Monthly Update 2021

SQA

EC Issues Notice on the Handling of Duplicate Marketing Authorization Applications (MAAs) of Pharmaceutical Products under Article 82(1) of Regulation (EC) No. The European Commission (EC) has issued a notice on the handling of duplicate MAAs of pharmaceutical products under Article 82(1) of Regulation (EC) No.