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HB3212 • 2025

Creates additional rules and requirements for pharmacy benefit managers and a policy or certificate of health insurance or other contract providing for the reimbursement of the cost of a prescription drug.

Creates additional rules and requirements for pharmacy benefit managers and a policy or certificate of health insurance or other contract providing for the reimbursement of the cost of a prescription drug.

Passed Legislature

This bill passed both chambers and reached final enrollment, even if later executive action is not shown here.

Sponsor
Representative Nosse,, Nathanson,, Diehl,, Levy B,, Smith G,, Wallan,, Senator Gelser Blouin,, Golden, Representative Boice,, Edwards,, Fragala,, Gamba,, Grayber,, Harbick,, Hudson,, Lewis,, Munoz,, Pham H,, Scharf,, Walters,, Watanabe,, Wright,, Senator Frederick,, Pham,, Prozanski,, Weber,
Last action
2025-06-27
Official status
In House Committee
Effective date
Not listed

Plain English Breakdown

Using official source text because the generated explanation was unavailable or could not be confirmed against the official bill text.

Creates additional rules and requirements for pharmacy benefit managers and a policy or certificate of health insurance or other contract providing for the reimbursement of the cost of a prescription drug.

Digest: Makes changes to the rules for PBMs and prescription drug benefits.

What This Bill Does

  • Digest: Makes changes to the rules for PBMs and prescription drug benefits.
  • (Flesch Readability Score: 64.9).
  • Creates additional rules and requirements for pharmacy benefit managers and a policy or certificate of health insurance or other contract providing for the reimbursement of the cost of a prescription drug.
  • Relating to: Relating to pharmacy benefits.

Limits and Unknowns

  • This entry is temporarily using official source text because the generated explanation could not be confirmed against the official bill text during the last sync.

Bill History

  1. 2025-06-27 House

    In committee upon adjournment.

  2. 2025-04-15 House

    Without recommendation as to passage and be referred to Rules.

  3. 2025-04-15 House

    Referred to Rules by order of Speaker.

  4. 2025-04-08 House

    Work Session held.

  5. 2025-02-04 House

    Public Hearing held.

  6. 2025-01-17 House

    Referred to Behavioral Health and Health Care.

  7. 2025-01-13 House

    First reading. Referred to Speaker's desk.

Official Summary Text

Digest: Makes changes to the rules for PBMs and prescription drug benefits. (Flesch Readability Score: 64.9).
Creates additional rules and requirements for pharmacy benefit managers and a policy or certificate of health insurance or other contract providing for the reimbursement of the cost of a prescription drug.
Relating to: Relating to pharmacy benefits.
Current location: In House Committee

Current Bill Text

Read the full stored bill text
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83rd OREGON LEGISLATIVE ASSEMBLY--2025 Regular Session
House Bill 3212
Sponsored by Representatives NOSSE, NATHANSON, DIEHL, LEVY B, WALLAN, Senators GELSER BLOUIN,
GOLDEN; Representatives GRAYBER, HUDSON, PHAM H, SCHARF, WRIGHT, Senators FREDERICK, PHAM
K, PROZANSKI, WEBER (Presession filed.)
SUMMARY
The following summary is not prepared by the sponsors of the measure and is not a part of the body thereof subject
to consideration by the Legislative Assembly. It is an editor’s brief statement of the essential features of the
measure as introduced. The statement includes a measure digest written in compliance with applicable readability
standards.
Digest: Makes changes to the rules for PBMs and prescription drug benefits. (Flesch Readability
Score: 64.9).
Creates additional rules and requirements for pharmacy benefit managers and a policy or cer-
tificate of health insurance or other contract providing for the reimbursement of the cost of a pre-
scription drug.
A BILL FOR AN ACT
Relating to pharmacy benefits; amending ORS 735.534 and 743A.062.
Be It Enacted by the People of the State of Oregon:
SECTION 1.
ORS 735.534, as amended by section 6, chapter 87, Oregon Laws 2024, is amended
to read:
735.534. (1) As used in this section:
[(a)(A)] (a) “Contract” does not mean a pharmacy or provider manual.
(b)(A) “Generally available for purchase” means a drug is available for purchase in this state
by a pharmacy from a national or regional wholesaler at the time a claim for reimbursement is
submitted by a network pharmacy.
(B) A drug is not “generally available for purchase” if the drug:
(i) May be dispensed only in a hospital or inpatient care facility;
(ii) Is unavailable due to a shortage of the product or an ingredient;
(iii) Is available to a pharmacy at a price that is at or below the maximum allowable cost only
if purchased in substantial quantities that are inconsistent with the business needs of a pharmacy;
(iv) Is sold at a discount due to a short expiration date on the drug; or
(v) Is the subject of an active or pending recall.
[(b)] (c) “List” means the list of drugs for which maximum allowable costs have been established.
[(c)] (d) “Maximum allowable cost” means the maximum amount that a pharmacy benefit man-
ager will reimburse a pharmacy for the cost of a drug.
[(d)] (e) “Multiple source drug” means a therapeutically equivalent drug that is available from
at least two manufacturers.
[(e)] (f) “Therapeutically equivalent” has the meaning given that term in ORS 689.515.
(2) A pharmacy benefit manager licensed under ORS 735.532:
(a) May not place a drug on a list unless there are at least two multiple source drugs, or at least
one generic drug generally available for purchase.
(b) Shall ensure that all drugs on a list are generally available for purchase.
(c) Shall ensure that no drug on a list is obsolete.
NOTE: Matter in boldfaced type in an amended section is new; matter [ italic and bracketed] is existing law to be omitted.
New sections are in boldfaced type.
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(d) Shall make available to each network pharmacy at the beginning of the term of a contract,
and upon renewal of a contract, the specific authoritative industry sources, other than proprietary
sources, the pharmacy benefit manager uses to determine the maximum allowable cost set by the
pharmacy benefit manager.
(e) Shall make a list available to a network pharmacy upon request in a format that:
(A) Is electronic;
(B) Is computer accessible and searchable;
(C) Identifies all drugs for which maximum allowable costs have been established; and
(D) For each drug specifies:
(i) The national drug code; and
(ii) The maximum allowable cost.
(f) Shall update each list maintained by the pharmacy benefit manager every seven business days
and make the updated lists, including all changes in the price of drugs, available to network phar-
macies in the format described in paragraph (e) of this subsection.
(g) Shall ensure that dispensing fees are not included in the calculation of maximum allowable
cost.
(h) May not reimburse a 340B pharmacy differently than any other network pharmacy based on
its status as a 340B pharmacy.
(i) Shall comply with the provisions of ORS 743A.062.
(j) May not retroactively deny or reduce payment on a claim for reimbursement of the cost of
services after the claim has been adjudicated by the pharmacy benefit manager unless the:
(A) Adjudicated claim was submitted fraudulently;
(B) Pharmacy benefit manager’s payment on the adjudicated claim was incorrect because the
pharmacy had already been paid for the services;
(C) Services were improperly rendered by the pharmacy in violation of state or federal law; or
(D) Payment was incorrect due to an error that the pharmacy and pharmacy benefit manager
agree was a clerical error.
(k) May not impose a fee on a pharmacy after the point of sale.
(L) Shall provide notice to a pharmacy of any claim for reimbursement of the cost of a pre-
scription drug that is denied or reduced. The notice shall identify the specific disaggregated claim
that was denied or reduced and a detailed explanation for why the specific claim was denied or re-
duced.
(m) May not engage in spread pricing.
(n) Shall pay a solo network pharmacy or a network pharmacy chain a professional dis-
pensing fee in an amount no less than the dispensing fee established by the Oregon Health
Authority by rule and reimburse the cost of the ingredients of the drug in an amount that
is the lesser of the following, but in no event less than the fee-for-service rate paid by the
authority for that specific drug in the medical assistance program:
(A) The pharmacy’s usual charge to the public for the drug; and
(B) The National Average Drug Acquisition Cost published by the Centers for Medicare
and Medicaid Services, or if the drug is not on the National Average Drug Acquisition Cost
rates list, the wholesale acquisition cost.
(o) Shall offer the same contract terms and options to network pharmacies and out-of-
network pharmacies, including reimbursing network and out-of-network pharmacies in the
same amount and manner for the same claims.
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(p) May not sign or enter into a contract with a pharmacy or pharmacy services admin-
istrative organization, as defined in section 2, chapter 87, Oregon Laws 2024, that:
(A) Requires a pharmacy to participate in any other contract;
(B) Restricts, prohibits or in any other way interferes with a pharmacist’s ability to
discuss the contract with any other individual or organization;
(C) Requires the pharmacy to meet unreasonable burdens, as defined by the Department
of Consumer and Business Services, including but not limited to requiring accreditation or
certification in addition to what is required by the Board of Pharmacy;
(D) Requires the pharmacy to provide pharmacist services to a patient if the pharmacy
will be reimbursed less than the pharmacy’s drug acquisition cost; or
(E) Requires the pharmacy to provide pharmacy services to an individual who no longer
has prescription drug benefit coverage.
(3) Subsection (2)(j) of this section may not be construed to limit pharmacy claim audits under
ORS 735.540 to 735.552.
(4) A pharmacy benefit manager must establish a process by which a network pharmacy may
appeal its reimbursement for a drug subject to maximum allowable cost pricing , ingredient cost
or dispensing fee . A network pharmacy may appeal a maximum allowable cost , ingredient cost
or dispensing fee if the reimbursement for the drug is less than the net amount that the network
pharmacy paid to the supplier of the drug. The process must allow a network pharmacy a period
of no less than 60 days after a claim is reimbursed in which to file the appeal. An appeal requested
under this section must be completed within 30 calendar days of the pharmacy making the claim for
which appeal has been requested.
(5) A pharmacy benefit manager shall allow a network pharmacy to submit the documentation
in support of its appeal on paper or electronically and may not:
(a) Refuse to accept an appeal submitted by a person authorized to act on behalf of the network
pharmacy;
(b) Refuse to adjudicate an appeal for the reason that the appeal is submitted along with other
claims that are denied; or
(c) Impose requirements or establish procedures that have the effect of unduly obstructing or
delaying an appeal.
(6) A pharmacy benefit manager must provide as part of the appeals process established under
subsection (4) of this section:
(a) A telephone number at which a network pharmacy may contact the pharmacy benefit man-
ager and speak with an individual who is responsible for processing appeals;
(b) A final response to an appeal of the reimbursement for a drug within seven business days;
and
(c) If the appeal is denied, the reason for the denial and the national drug code of a drug that
may be purchased by similarly situated pharmacies at a price that is equal to or less than the
maximum allowable cost.
(7)(a) If an appeal is upheld under this section, the pharmacy benefit manager shall:
(A) Make an adjustment for the pharmacy that requested the appeal from the date of initial
adjudication forward; and
(B) Allow the pharmacy to reverse the claim and resubmit an adjusted claim without any addi-
tional charges.
(b) If the request for an adjustment has come from a critical access pharmacy, as defined by the
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Oregon Health Authority by rule for purposes related to the Oregon Prescription Drug Program, the
adjustment approved under paragraph (a) of this subsection shall apply only to critical access
pharmacies.
(8) A pharmacy may file a complaint with the Department of Consumer and Business Services
to contest a finding of a pharmacy benefit manager in response to an appeal under subsection (4)
of this section or a pharmacy benefit manager’s failure to comply with the provisions of this section.
(9) The Department of Consumer and Business Services may adopt rules to carry out the pro-
visions of this section.
SECTION 2.
ORS 743A.062, as amended by section 11, chapter 87, Oregon Laws 2024, is
amended to read:
743A.062. (1) As used in this section:
(a) “Medical assistance program” means the state program that provides medical assistance as
defined in ORS 414.025.
(b) “340B drug” means a covered drug dispensed by a covered entity, as those terms are defined
in 42 U.S.C. 256b, that is subject to the cap on amounts required to be paid in 42 U.S.C. 256b(a)(1).
(2) A policy or certificate of health insurance or other contract providing for the reimbursement
of the cost of a prescription drug to a resident of this state [ may not]:
(a) May not exclude coverage of the drug for a particular indication solely on the grounds that
the indication has not been approved by the United States Food and Drug Administration if the
Health Evidence Review Commission established under ORS 414.688 or the Pharmacy and
Therapeutics Committee established under ORS 414.353 determines that the drug is recognized as
effective for the treatment of that indication:
(A) In publications that the commission or the committee determines to be equivalent to:
(i) The American Hospital Formulary Service drug information;
(ii) “Drug Facts and Comparisons” (Lippincott-Raven Publishers);
(iii) The United States Pharmacopoeia drug information; or
(iv) Other publications that have been identified by the United States Secretary of Health and
Human Services as authoritative;
(B) In the majority of relevant peer-reviewed medical literature; or
(C) By the United States Secretary of Health and Human Services;
(b) For an insured who is enrolled in the medical assistance program, may not :
(A) Except as provided in subsection (3) of this section, require a prescription for the drug to
be filled or refilled at a mail order pharmacy; or
(B) Require a prescription for the drug to be filled or refilled at a pharmacy that is not a local
pharmacy enrolled in the medical assistance program;
(c) May not discriminate in the reimbursement of a prescription for 340B drugs from other
prescription drugs;
(d) May not assess a fee, chargeback, clawback or other adjustment for the dispensing of a 340B
drug;
(e) May not exclude a pharmacy from a pharmacy network on the basis that the pharmacy
dispenses a 340B drug;
(f) May not restrict the methods by which a 340B drug may be dispensed or delivered; [ or]
(g) May not restrict the number of pharmacies within a pharmacy network that may dispense
or deliver 340B drugs[ .];
(h) Must permit the policyholder, certificate holder or beneficiary, at the time of issu-
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ance, amendment or renewal, to select a licensed pharmacy or licensed pharmacist for the
dispensing of prescription drugs reimbursed by the policy, certificate or contract;
(i) May not deny a pharmacy or pharmacist licensed in this state the opportunity to
participate as a preferred provider or a contracting provider under the same terms and
conditions applicable to all other preferred or contracting providers if the pharmacy or
pharmacist agrees to the terms and conditions; or
(j) May not require beneficiaries to fill prescriptions at network pharmacies, as defined
in ORS 735.530.
(3) Subsection (2)(b)(A) of this section does not prohibit an insurer from requiring a medical as-
sistance recipient to fill or refill a prescription for a specialty drug at a mail order pharmacy that
is a specialty pharmacy.
(4) Required coverage of a prescription drug under this section shall include coverage for med-
ically necessary services associated with the administration of that drug.
(5) Nothing in this section requires coverage for any prescription drug if the United States Food
and Drug Administration has determined use of the drug to be contraindicated.
(6) Nothing in this section requires coverage for experimental drugs not approved for any indi-
cation by the United States Food and Drug Administration.
(7) Notwithstanding ORS 750.055 (1)(h), this section does not apply to a health maintenance or-
ganization as defined in ORS 750.005.
(8) This section is exempt from ORS 743A.001.
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