Welcome to your daily briefing on healthcare developments in North Carolina. Today we're covering 7 key stories including updates on north carolina healthcare headlines, background & context. Let's dive in.
4 stories
The North Carolina Department of Health and Human Services outlines its mission to safeguard the well-being of all state residents.
This establishes the regulatory and service framework that healthcare professionals in NC must adhere to for compliance and patient care.
The North Carolina Medical Board was created to properly regulate the practice of medicine and surgery for the benefit and protection of the people of North Carolina.
This regulatory body oversees the standards and conduct of medical professionals within the state, ensuring patient safety and professional accountability.
The North Carolina Department of Health and Human Services is inaugurating a new electronic health records system for its state-operated facilities, aiming to advance patient communication and care.
This rollout represents a significant operational shift for healthcare professionals within the state's public health network, potentially altering data access and patient interaction workflows.
State and Federal Health Departments and Divisions Who Does What? NCIOM has compiled a list of state and federal health departments and divisions, along with short descriptions of their...
Relevant to healthcare professionals operating in NC.
Reach healthcare professionals
3 stories
A vendor is a business associate if they create, receive, maintain, or transmit PHI on behalf of the covered entity. They are NOT a business associate just because they happen to be in a building with PHI or could conceivably access it. The functional test matters, not the proximity test.
Forcing BAA execution on vendors who do not meet the functional test creates contractual bloat and weakens the negotiating position with vendors who actually do. Failing to execute BAAs with true business associates exposes the covered entity to OCR enforcement.
OSHA inspections of healthcare facilities most commonly find three violations: an Exposure Control Plan that has not been reviewed annually (date-stamped review required), engineering controls that have not been re-evaluated when new devices are introduced, and post-exposure protocols that do not match the actual reporting workflow.
Each citation carries per-violation penalties, and willful or repeat designations multiply them. Re-evaluation paperwork is the cheapest control to maintain.
The No Surprises Act good-faith-estimate requirement applies to all licensed providers offering services to self-pay or uninsured patients — not just hospitals or large groups. The estimate must be provided within timeframes that vary by how far in advance the appointment is scheduled.
Patient-provider dispute resolution under NSA typically defaults to the patient when the practice cannot produce a timely good-faith estimate. The penalty is the full disputed amount being struck.
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