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HB 2176

In Committee

House

Drug therapy agreements/PRA

Exempting information in collaborative drug therapy agreements from disclosure under the public records act.

  1. Introduced (completed)
  2. 2
    Committee (current stage)
  3. 3
    Floor Vote (not started)
  4. 4
    Opposite Chamber (not started)
  5. 5
    Governor (not started)
  6. 6
    Signed (not started)

This status may be delayed. See Action History below for the latest updates.

How does a bill become law?
  1. Introduced: The bill is filed and assigned a number.
  2. Committee: A subject-matter committee holds hearings, takes public testimony, and decides whether to advance the bill.
  3. Floor Vote: The full chamber (House or Senate) debates and votes on the bill.
  4. Opposite Chamber: The bill repeats the committee and floor vote process in the other chamber.
  5. Governor: The Governor reviews the bill and decides whether to sign or veto it.
  6. Signed: The bill has been signed into law.
Introduced: January 11, 2026
Last Action: February 19, 2026
Status: H Rules X

AI Analysis

This analysis was generated by AI and may contain errors. It is not legal advice. Always refer to the official bill text for authoritative information.
People & CommunitiesPeople-leaningCorporate & Wealthy Interests

This bill makes collaborative drug therapy agreements (CDTAs) — written agreements between pharmacists and prescribers that outline how medications are managed — confidential and exempt from public disclosure, except when the agreement is used in a disciplinary case against a licensed provider. It also protects the personal details of individuals involved, unless they are the subject of the disciplinary action.

  • Adds collaborative drug therapy agreements (CDTAs) and their attachments to the list of health information exempt from public disclosure under the Public Records Act.
  • Allows CDTAs to be disclosed only if they are used as evidence in a disciplinary action against a licensed health care provider (e.g., pharmacists, prescribers); in such cases, only the disciplined provider’s personally identifiable information may be included in the disclosure.
  • Protects personally identifiable information (e.g., names, addresses, credential numbers, email addresses, facility addresses and phone numbers) of individuals other than the disciplined provider, even if the CDTA itself is disclosed.
  • Clarifies that confidentiality applies regardless of which state agency holds the CDTA documents.

Who is affected

  • Pharmacists and prescribers using collaborative drug therapy agreements — Pharmacists and other health care providers who enter into collaborative drug therapy agreements (CDTAs) with prescribers; their agreement content and associated personally identifiable information may be protected from public disclosure unless used in a disciplinary case.
  • Patients — Patients whose information may be included in CDTAs; their personally identifiable details are protected from disclosure even if the agreement itself is disclosed due to a disciplinary action.
  • State health regulatory agencies (PQAC and DOH) — The Pharmacy Quality Assurance Commission (PQAC) and Department of Health, which collect and manage CDTAs and related health data; they must follow new confidentiality rules when handling such records.
  • Public records requesters (e.g., journalists, researchers, citizens) — Members of the public or news organizations seeking access to health care records; they will no longer be able to obtain CDTAs (or certain other health data) through public records requests, except under limited circumstances.
Effective: July 28, 2026
Model: Intel/Qwen3-Coder-Next-int4-AutoRoundGenerated: Mar 20, 2026, 2:42 AM

Pro/Con Analysis

Potential Benefits (5)
  • Protects the privacy of non-disciplined individuals (e.g., pharmacists, other prescribers) named in CDTAs — preventing reputational harm, harassment, or unwarranted scrutiny if their involvement in a collaborative agreement becomes public, even when no misconduct occurred.

    Rights & LibertiesPeopleRef: Sec. 1(6)(b)-(c)
  • Safeguards patient privacy by ensuring that CDTAs — which may contain detailed medication histories, dosing regimens, and provider-patient interactions — are not publicly exposed, reducing risk of identity theft, discrimination, or stigmatization.

    Rights & LibertiesPeopleRef: Sec. 1(6)(a)
  • Encourages candid, open collaboration between pharmacists and prescribers by reducing fear of public exposure or misinterpretation of complex medication management plans — potentially improving adherence and outcomes in chronic disease management.

    HealthcarePeopleRef: Sec. 1(6)(a)
  • Prevents accidental disclosure of sensitive facility contact details (e.g., pharmacy phone numbers, practice site addresses) that could be used for harassment or fraud if made public — especially important in rural or small communities where provider identities are easily linkable.

    HealthcareLean peopleRef: Sec. 1(6)(c)
  • May reduce legal exposure for providers by preventing out-of-context quoting or selective publication of CDTA terms — though this benefit is modest and speculative, as CDTAs are already subject to professional standards review.

    HealthcareLean peopleRef: Sec. 1(6)(a)
Potential Concerns (5)
  • Withholding CDTAs from public disclosure reduces transparency around medication safety incidents and provider conduct, potentially limiting public awareness of systemic risks (e.g., repeated prescribing errors, unsafe collaboration patterns) unless a disciplinary action occurs — and even then, only the disciplined provider’s identity is revealed, not the full context.

    Public SafetyPeopleRef: Sec. 1(6)(a)-(b)
  • Even when CDTAs are disclosed in disciplinary cases, personally identifiable information of non-disciplined individuals (e.g., pharmacists, other prescribers involved in the same agreement) is protected — obscuring accountability for shared responsibility and hindering public or peer analysis of collaborative failures.

    Public SafetyPeopleRef: Sec. 1(6)(b)-(c)
  • By making CDTAs confidential by default, the bill removes a key source of data for researchers, journalists, and public health agencies seeking to identify patterns of medication errors, inappropriate prescribing, or pharmacy practice risks — limiting early intervention and system-level improvements.

    Public SafetyPeopleRef: Sec. 1(6)(a)
  • The narrow exception for disclosure in disciplinary cases creates a high bar for public scrutiny — only after a formal finding of misconduct is made, and only for the disciplined provider, meaning most CDTAs (including those involving near-misses or systemic issues without formal discipline) remain hidden.

    Public SafetyPeopleRef: Sec. 1(6)(b)
  • The definition of “personally identifiable information” excludes identifiers like license numbers and facility addresses — which, while sensitive, could be de-identified for research or oversight purposes — thus overbroad in protecting information that does not meaningfully threaten privacy if anonymized.

    Public SafetyLean peopleRef: Sec. 1(6)(c)

Who Is Most Affected

  • Pharmacists and prescribers using collaborative drug therapy agreementsMixed Impact

    Pharmacists and prescribers benefit from stronger privacy protections, especially when involved in collaborative agreements that later face scrutiny — but may face reduced public trust if errors are hidden, and may have less incentive to document thoroughly if agreements are not subject to oversight.

  • PatientsMixed Impact

    Patients gain privacy and protection from potential stigma or discrimination tied to their medication regimens — but lose the benefit of public oversight that could expose unsafe or inappropriate prescribing practices affecting them or others.

  • State health regulatory agencies (PQAC and DOH)Mixed Impact

    Regulatory agencies gain operational flexibility by limiting disclosure burdens, but lose a valuable data source for identifying trends and enforcing standards — potentially weakening their ability to proactively prevent harm.

  • Public records requesters (e.g., journalists, researchers, citizens)Negative Impact

    Journalists, researchers, and citizens lose a tool for accountability and public health investigation — especially impactful in cases where disciplinary actions are rare or settlements are confidential, hiding systemic issues from public view.

Sponsors

  • Representative Thai(Democrat)District 41Primary
  • Representative Parshley(Democrat)District 22Secondary
  • Representative Ryu(Democrat)District 32Secondary
  • Representative Reed(Democrat)District 36Secondary
  • Representative Zahn(Democrat)District 41Secondary
  • Representative Gregerson(Democrat)District 33Secondary
  • Representative Reeves(Democrat)District 30Secondary
  • Representative Fosse(Democrat)District 38Secondary