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What is GRC in Healthcare?

Verisys

This includes clinical risks, financial risks, cybersecurity threats, and compliance risks with laws and regulations such as HIPAA (Health Insurance Portability and Accountability Act) in the United States. For instance, within the realm of healthcare compliance, HIPAA compliance plays a pivotal role.

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Who Is Responsible For Compliance In Healthcare?

MedTrainer

Healthcare Compliance Complexities The first healthcare compliance programs began in the early 20th century as a response to concerns about the quality of care provided by medical practitioners. Licensing and credentialing were introduced to regulate healthcare professionals and ensure minimum standards of care.

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OIG Issues Final Information Blocking Enforcement Rule and Highlights the Potential for Referrals to the FTC and FCA Liability

Health Care Law Brief

Specifically, OIG signaled that “unconscionable or one-sided business terms for the access, exchange, or use of EHI, or the licensing of an interoperability element” may rise to the level of information blocking if the conduct “impedes a provider’s ability to care for patients.” [4]

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EU and US Regulatory Challenges Facing AI Health Care Innovator Firms

Bill of Health

Although the cross-sectoral AI legislation that is now introduced by the European Commission’s Digital Strategy aims to be integrated with existing sectoral legislation such as the MDR, the IVDR and the Machinery Directive, it is uncertain how overlapping regulatory compliance requirements for AI-driven medical devices will be managed in practice.

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How to Choose the Right eQMS – The Ultimate Guide

Dot Compliance

In the highly regulated life sciences industry, quality management is crucial for ensuring product safety, regulatory compliance, and operational excellence. It could be improving product safety, enhancing regulatory compliance, streamlining processes, increasing efficiency, or reducing quality-related risks.

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How to Choose the Right QMS – The Ultimate Guide

Dot Compliance

In the highly regulated life sciences industry, quality management is crucial for ensuring product safety, regulatory compliance, and operational excellence. It could be improving product safety, enhancing regulatory compliance, streamlining processes, increasing efficiency, or reducing quality-related risks.

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Takeaways from OCR’s Right of Access Initiative: Additional Enforcement Actions Demonstrate Ongoing Risks of Noncompliance

Hall Render

Department of Health and Human Services (“HHS”) announced its resolution of eleven separate investigations against covered entities for violations of the individual’s right of access under the Health Insurance Portability and Accountability Act of 1996 (“HIPAA”). Click here for a summary of the recent enforcement actions.

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