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Introductory Editorial — Critical Psychedelic Studies: Correcting the Hype

Bill of Health

By Neşe Devenot Since the 2022 publication of “ Preparing for the Bursting of the Psychedelic Hype Bubble ,” a JAMA Psychiatry Viewpoint by David Yaden and colleagues, a wave of scholarship and commentaries has emphasized the ethical importance of nuanced science communication about the still-nascent field of psychedelic medicine.

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Update on No Surprises Act 2022

AIHC

Written by: Joanne Byron , BS, LPN, CCA, CHA, CHCO, CHBS, CHCM, CIFHA, CMDP, COCAS, CORCM, OHCC, ICDCT-CM/PCS As a result of the 2021 Consolidated Appropriations Act, several No Surprises Billing Act regulations went into effect on January 1, 2022, for providers, facilities and air ambulance services.

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Could Self-Operated Assisted Suicide Devices Be Coming to a Town near You?

Bill of Health

While not exhaustive, this blog post explores some of the major legal issues likely to arise if a device like the Sarco were to be introduced into the United States. As of May 2022, physician-assisted suicide is legal in ten U.S. Under the U.S. Federal Considerations. FDA Approval. A natural place to begin is the U.S.

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What Are the Main Types of Healthcare Incidents?

MedTrainer

Food and Drug Administration Patient Rights Violations Incidents involving breaches of patient confidentiality, informed consent issues, or disregard for patient autonomy and dignity. million in 2022. Fact: In 2023, hackers and thieves exposed, stole, or impermissibly disclosed 133 million patients records. There were 45.9

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SQA Regulatory Surveillance Summary | Monthly Update 2022 – Spring

SQA

SQA Regulatory Surveillance Summary 2022 – Spring. Brazil’s ANVISA Issues Registration Rules for Software, 01 April 2022. ANVISA has published new regulations focused on software as a medical device (SaMD), set to take effect on 01 July 2022. Agência Nacional de Vigilância Sanitária (ANVISA).

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SQA Regulatory Surveillance Summary | Monthly Update 2023 – January

SQA

Relevant matters are hereby announced as follows: As of 01 December 2022, the Electronic Certificates of Documentation for Export of APIs to the EU and Certificate of a Pharmaceutical Product will be put into use. Efforts should be made to promote and guide the use of electronic certificates.

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Part 3: An Update on the Federal and State E-Roe-sion or P-Roe-tection of Abortion Rights

Healthcare Law Blog

The now-active provisions include a prohibition on abortions after 12 weeks of pregnancy (with limited exceptions), 72-hour informed consent requirements, pre-abortion gestational age verification, and reporting requirements for abortions after 12 weeks. [21] 5, 2022 Leg., 10, 2022). LEXIS 61474, at *96 (N.D. 7, 2023).