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EU and US Regulatory Challenges Facing AI Health Care Innovator Firms

Bill of Health

Beyond the health care sector-specific Medical Devices Regulation (EU) 2017/745 (MDR) and the In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746 (IVDR), this mix of AI & Data related regulatory requirements stems from a series of generalized, cross-sectoral EU laws of the last 5 years.

FDA 282
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Managing Healthcare Compliance in Florida

MedTrainer

Its departments, like the Office of Compliance, diligently uphold ethical standards, integrity, and regulatory compliance. Ensuring adherence to licensing requirements, the Florida Agency for Health Care Administration oversees Medicaid, coordinating essential healthcare access to vulnerable populations.

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

Drug & Device Law

Negligence requires an evaluation of a defendant’s reasonableness, and all relevant NC authority includes relevant regulatory compliance in that mix. If compliance isn’t preemptive in a medical device case, then these cases conclude it isn’t admissible at all. Hrymoc was tried in late 2017. Strike one. 13) McGee v.

FDA 105