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SQA Regulatory Surveillance Summary | Monthly Update 2022 – Spring

SQA

For Investigator Sites, the subject areas are Organizational Aspects, Informed Consent of Trial Participants, Review of Trial Participant Data, and Management of Investigational Medicinal Product(s). United States Food and Drug Administration (FDA) – Regulations and Guidances.

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Health Provider News – February 10, 2023

Hall Render

leading cause of death is heart disease, Alabama’s matches that Alabama lawmakers put temporary hold on $1 billion contract for prison healthcare New rolling NICU a ‘game changer’ for critical babies in Alabama More than a dozen Alabama hospitals at immediate risk of closing; officials say hospitals suffer $1.5

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Health Care Is Front and Center as DeSantis and Newsom Go Mano a Mano

Kaiser Health News

He also approved $60 million to help uninsured patients and people from out of state pay for abortions in California, and signed reproductive health care laws, including one protecting doctors who mail abortion pills to other states. The Golden State’s covid-19 vaccine booster rate for residents ages 5 and older is 21.9%.

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Suing the Certifiers – A Dangerous Undertaking

Drug & Device Law

Apparently, a fraudulent foreign-trained “doctor” treated the plaintiffs, none of whom claimed malpractice or any physical injury whatsoever. Anyway, this fraudulent “doctor” allegedly “touched them without informed consent” and caused them “emotional distress. University Hospital , 659 N.Y.S.2d 2d 395, 399 (N.Y.

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FDA Safety Communication Not Enough to Support Punitive Damages Claim in New Jersey

Drug & Device Law

But it involves the interplay between an FDA “Safety Communication” and punitive damages, so we thought it was worth looking at. Valley Hospital, Inc. The FDA data showed that approximately.28% One month after the update, the hospital discontinued use of the device. Notably, the FDA Communication was not enough.

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