Remove Doctors Remove Informed Consent Remove Licensing Remove Nursing Homes
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SQA Regulatory Surveillance Summary | Monthly Update 2022 – Spring

SQA

The Points is an upgraded version of Practice for Cosmetics Production Licensing , implemented in 2016, with more stringent inspection requirements. Patients currently taking the products should consult with their doctor or healthcare provider about alternative treatment options.

FDA 75
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Health Provider News – February 10, 2023

Hall Render

deal to buy national physician practice Support grows for association health plans as small employer insurance costs soar Connecticut doctors call on legislature to tackle prior authorization during this year’s session CT hospitals support student-loan forgiveness, debt-free college programs to boost healthcare workforce DC D.C.’s

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

Drug & Device Law

Plaintiff knew about it, too, since he signed an informed consent document mentioning it. Equally bad, Hrymoc effectively read a New Jersey statute, §2A:58C-5(c), which precludes punitive damages where a “device” was “licensed” by the FDA, out of existence. The device labeling specifically mentioned it.

FDA 105