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HB 1019

Health Coordination Network Program; patient data collection.

2026 Regular Session Introduced by Atoosa Reaser

Virginia bill HB 1019 creates a statewide Health Coordination Network Program enabling healthcare providers to collect and share patient data to improve care coordination and outcomes.

Approved by Governor-Chapter 930 (effective 7/1/2026)
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Bill Summary · HB 1019

Legislative bill overview

HB 1019 establishes a Health Coordination Network Program in Virginia that creates a framework for collecting and sharing patient data across healthcare providers and systems. The bill appears designed to improve care coordination by enabling authorized entities to access standardized patient health information for treatment and program purposes.

Why is this important

Better health data coordination can reduce duplicate tests, improve medication management, and enhance outcomes for patients with complex or chronic conditions. However, this requires balancing improved care efficiency against patient privacy concerns and the risk of unauthorized data access or misuse.

Potential points of contention

  • Data privacy and security standards — The scope of data collection, who can access patient information, and what safeguards prevent misuse or breaches remain unclear from the bill's current status
  • Patient consent requirements — Whether patients must explicitly opt-in to data sharing or if participation is automatic/opt-out could significantly affect voluntary participation rates
  • Implementation costs and burden — Healthcare providers may face substantial expenses to integrate with the network, potentially affecting smaller practices disproportionately
  • Governance and oversight — Questions about which entity manages the network, how disputes are resolved, and enforcement mechanisms for compliance aren't yet detailed in available materials

Compiled from official sources — confirm details with the bill’s official record.

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