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SB 341 DE
Passed Legislature

AN ACT TO AMEND TITLE 16 OF THE DELAWARE CODE RELATING TO THE DELAWARE HEALTH INFORMATION NETWORK.

DE · session 153 · Senate · bill

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Introduced Jun 4, 2026

Latest action (Jun 24, 2026) Passed By House. Votes: 37 YES 1 NO 3 ABSENT

Summary

This bill designates the Delaware Health Information Network (DHIN) as the state's sanctioned provider of Health Data Utility services and clarifies its authority to contract with other organizations in furtherance of its mission. The bill aligns DHIN's use of health data with federal requirements for research and analytics purposes under HIPAA and the Common Rule. The bill also clarifies that patients have access to clinical information from claims data included in their longitudinal health records, excluding pricing information. Additionally, it specifies that state agencies may access standardized claims data sets curated by DHIN at no cost.

AI-generated plain-language summary of the bill (from the OpenStates abstract — no full text available yet) — neutral, and may be imperfect.

Official abstract

Sections 1 and 2 of this Act identify DHIN as the State’s sanctioned provider of Health Data Utility (HDU) services. The HDU concept arises and builds off of services provided by Health Information Exchanges (HIEs) such as DHIN. Including this language will align with DHIN’s development and assist the State in responding to federal and other grant funding opportunities that require or prefer collaboration with a sanctioned HDU. Section 2 of this Act is a clarifying provision that states DHIN’s ability to contract with organizations in furtherance of its mission in business arrangements that facilitate DHIN’s underlying mission, notwithstanding that those organizations may provide services (such as direct provision of treatment to patients) that DHIN does not directly provide under this chapter. It also makes a technical change to align the list of stakeholders identified with lists that appear elsewhere in the statute. Section 3 of this Act aligns DHIN’s use cases more clearly with the requirements of federal law that relate to using health data for analytic and research purposes, including the Health Insurance Portability and Accountability Act of 1996 (HIPAA) and the Federal Policy for Protection of Human Subjects (the Common Rule) and makes a technical correction to a description of DHIN processes. This change will also ensure consistency between permitted uses of claims data for research purposes and permitted uses of clinical data. Sections 4 and 5 clarify DHIN’s ability to incorporate clinically relevant information into a patient’s longitudinal record, excluding pricing information, for access as permitted by the laws and regulations governing DHIN’s HIE services. This clarification ensures patients will have access to the clinical information included in claims data for their own uses. Section 5 makes a technical correction to recognize that DHIN’s enabling legislation and applicable federal law do not permit DHIN to “report” data to the public that would be suitable for the public health improvement research and activities purposes designed to be encouraged by that section, and clarifies that the identified agencies will have access to the standardized claims data sets curated by DHIN from the Delaware Health Care Claims Database as otherwise permitted under this statute at no cost.

Sponsors (4)

Action history (6)

  1. Jun 4, 2026 Introduced and Assigned to Health & Social Services Committee in Senate · upper
  2. Jun 10, 2026 Reported Out of Committee (Health & Social Services) in Senate with 3 Favorable, 3 On Its Merits · upper
  3. Jun 11, 2026 Passed By Senate. Votes: 20 YES 1 ABSENT · upper
  4. Jun 11, 2026 Assigned to Health & Human Development Committee in House · lower
  5. Jun 18, 2026 Reported Out of Committee (Health & Human Development) in House with 9 On Its Merits · lower
  6. Jun 24, 2026 Passed By House. Votes: 37 YES 1 NO 3 ABSENT · lower

Full text

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