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May 2024 Regulatory Compliance Updates

Verisys

– The best resource for monthly healthcare regulatory compliance updates. Compliance Updates: May 2024 Overlook: Board Updates Arizona : Legislation has been passed to update the requirements of Physician Assistants and supervision requirements. This legislation also updates the definition and details of supervision agreement.

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Who Is Responsible For Compliance In Healthcare?

MedTrainer

Healthcare compliance. Just as perplexing is who is responsible for compliance in healthcare organizations. The answer has as many layers as the definition of compliance itself. The answer has as many layers as the definition of compliance itself. And they’d be partly right.

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DEA Information for Dental Healthcare Practitioners Training

American Medical Compliance

As dental healthcare practitioners, understanding the regulations and guidelines set forth by the Drug Enforcement Administration (DEA) is crucial for maintaining compliance and ensuring safe prescribing practices. To become certified, please visit us at American Medical Compliance (AMC). One is credentialing and licensing.

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From Discretion to Regulation: What FDA’s Final Rule Means for Laboratory Developed Tests

Hall Render

In April 2024, the Food and Drug Administration (“FDA”) issued a Final Rule amending the definition of in vitro diagnostics products (“IVDs”) found in 21 C.F.R. To learn more about the significance of the FDA’s New Rule, join Hall Render attorneys on June 11 at 1:00 PM ET for a 60-minute webinar.

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Artificial Intelligence (AI) and Advancing Quality of Care

AIHC

This definition focuses on the outcomes of the diagnostic process, recognizing that diagnosis is an iterative process that solidifies as more information becomes available. Read more about current regulatory oversight on the AIHC blog: Who Regulates Healthcare AI?

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Healthcare Interoperability, Data, and Cloud – 2024 Health IT Predictions

Healthcare IT Today

Clinicians need to spend their 10-15 minutes in an exam room talking to patients, answering questions, and practicing at the top of their license. As a result, proactive compliance around the handling of ePHI will be more important than ever for the healthcare industry this year.

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SQA Regulatory Surveillance Summary | Monthly Update 2022 – July/August

SQA

The counterfeit devices were sold online by a distributor named Healthful Plus without the required license to import, distribute, or sell medical devices in Canada. The packaging of the counterfeit kits resembles authentic (licensed) BTNX Inc. Medicines and Healthcare Products Regulatory Agency (MHRA) . Health Advance Inc.