Pennsylvania Act 2016-169 — PHARMACY BENEFIT REFORM ACT - ENACTMENT

Act text

AN ACT

Providing for pharmacy audit procedures, for registration of pharmacy benefits managers and auditing entities, for maximum allowable cost transparency, for prescription drugs reimbursed under the PACE and PACENET program and for pharmacy benefit managers contract requirements and prohibited activities; and making related repeals. (Title amended July 17, 2024, P.L.852, No.77)

TABLE OF CONTENTS

Chapter 1. Preliminary Provisions

Section 101. Short title.

Section 102. Scope of act.

Section 103. Definitions.

Section 104. Regulations.

Chapter 3. Pharmacy Audits

Section 301. Procedures for conducting pharmacy audits.

Section 302. Appeals process.

Section 303. Limitations.

Section 304. Regulations.

Chapter 5. Registration

Section 501. PBM and auditing entity registration.

Chapter 6. Pharmacy Benefits Manager Contracts

Section 601. Contract provisions.

Section 602. Patient steering.

Section 603. Clawbacks prohibited.

Section 604. Network adequacy.

Chapter 7. PBM Cost Transparency Requirements

Section 701. Multiple source generic list and reimbursement.

Section 702. Availability of multiple source generic list.

Section 703. Multiple source drug pricing appeals process.

Section 703.1. PBM transparency report required.

Section 704. Regulations (Repealed).

Section 704.1. PSAO reporting requirements.

Section 705. Applicability.

Chapter 8. PACE and PACENET Program Payments

Section 801. Definitions.

Section 802. Program payment.

Section 803. Generic drugs.

Chapter 9. Enforcements

Section 901. Scope of enforcement authority.

Chapter 10. Pharmacy Services

Section 1001. Definitions.

Section 1002. Administration of injectable medications, biologicals and immunizations.

Section 1003. Clinical laboratory certificate.

Section 1004. Report on pharmacy-administered vaccines.

Chapter 11. Miscellaneous Provisions

Section 1101. Repeals.

Section 1102. Effective date.

The General Assembly of the Commonwealth of Pennsylvania hereby enacts as follows:

CHAPTER 1

PRELIMINARY PROVISIONS

Section 101. Short title.

This act shall be known and may be cited as the Pharmacy Benefit Reform Act.

(101 amended July 17, 2024, P.L.852, No.77)

Section 102. Scope of act.

The following apply:

(1) This act covers any audit of the records of a pharmacy conducted by a managed care company, third-party payer, pharmacy benefits manager or an entity that represents a covered entity.

(2) This act covers any contract between a pharmacy or a PBM and a health insurer or a health benefit plan, or a contract between a pharmacy and a PBM on behalf of a health insurer or health benefit plan.

(3) Except for the provisions of Chapter 5, this act shall not apply to a self-insured health benefit plan subject to ERISA or exempted from ERISA under section 4(b) of ERISA.

(102 amended July 17, 2024, P.L.852, No.77)

Section 103. Definitions.

The following words and phrases when used in this act shall have the meanings given to them in this section unless the context clearly indicates otherwise:

"Affiliate" or "affiliated." An affiliate as defined in section 1401 of the act of May 17, 1921 (P.L.682, No.284), known as The Insurance Company Law of 1921. (Def. added July 17, 2024, P.L.852, No.77)

"Auditing entity." A person or company that performs a pharmacy audit, including a covered entity, pharmacy benefit manager, managed care organization or third-party administrator.

"Business day." Any day of the week excluding Saturday, Sunday and any legal holiday.

"Complex or chronic medical condition." A physical, behavioral or developmental condition that has no known cure, is progressive or can be debilitating or fatal if unmanaged or untreated. (Def. added July 17, 2024, P.L.852, No.77)

"Covered entity." A contract holder or policy holder providing pharmacy benefits to a covered individual under a health benefit plan pursuant to a contract administered by a pharmacy benefit manager. (Def. amended July 17, 2024, P.L.852, No.77)

"Covered individual." A member, participant, enrollee or beneficiary of a covered entity who is provided health coverage by the covered entity. The term includes a dependent or other person provided health coverage through the policy or contract of a covered individual.

"Department." The Insurance Department of the Commonwealth.

"ERISA." The Employee Retirement Income Security Act of 1974 (Public Law 93-406, 29 U.S.C. § 1001 et seq.). (Def. added July 17, 2024, P.L.852, No.77)

"Extrapolation." The practice of inferring a frequency of dollar amount of overpayments, underpayments, nonvalid claims or other errors on any portion of claims submitted, based on the frequency of dollar amount of overpayments, underpayments, nonvalid claims or other errors actually measured in a sample of claims.

"Health benefit plan." A policy, contract or certificate entered into, offered, issued or renewed by a health insurer to provide, deliver, arrange for, pay for or reimburse any of the costs of physical, mental or behavioral health care services. The term does not include Medicare supplement or accident only, fixed indemnity, limited benefit, credit, dental, vision, specified disease, TRICARE supplemental insurance, long-term care or disability income, workers' compensation or automobile medical payment insurance. (Def. added July 17, 2024, P.L.852, No.77)

"Health care practitioner." As defined in section 103 of the act of July 19, 1979 (P.L.130, No.48), known as the Health Care Facilities Act.

"Health insurance policy." (Def. deleted by amendment July 17, 2024, P.L.852, No.77)

"Health insurer." An entity licensed by the department with authority to issue a policy, subscriber contract, certificate or plan that provides prescription drug coverage that is offered or governed under any of the following:

(1) The act of May 17, 1921 (P.L.682, No.284), known as The Insurance Company Law of 1921, including section 630 and Article XXIV thereof.

(2) The act of December 29, 1972 (P.L.1701, No.364), known as the Health Maintenance Organization Act.

(3) 40 Pa.C.S. Ch. 61 (relating to hospital plan corporations) or 63 (relating to professional health services plan corporations).

"Health insurer client." The term includes both a health insurer and a health benefit plan offered by a health insurer. (Def. added July 17, 2024, P.L.852, No.77)

"Licensee or registrant." An entity subject to oversight of the department under this act. The term includes:

(1) An auditing entity.

(2) A health insurer.

(3) A pharmacy benefit manager.

(4) A pharmacy services administration organization.

(Def. added July 17, 2024, P.L.852, No.77)

"Mail order pharmacy." A pharmacy where prescriptions are dispensed to covered individuals via the mail. (Def. added July 17, 2024, P.L.852, No.77)

"Maintenance medication." A medication prescribed for a chronic, long-term condition and taken on a regular, recurring basis. (Def. added July 17, 2024, P.L.852, No.77)

"Maximum allowable cost." The maximum amount that a pharmacy benefits manager will reimburse a pharmacy for the cost of a drug or a medical product or device.

"Multiple source drug." A covered outpatient drug for which there is at least one other drug product that is rated as therapeutically equivalent under the Food and Drug Administration's most recent publication of "Approved Drug Products with Therapeutic Equivalence Evaluations."

"Multiple source generic list." A list of drugs, medical products or devices, or both, for which a maximum allowable cost has been established by a pharmacy benefits manager.

"Network." A pharmacy or group of pharmacies that agrees to provide prescription services to covered individuals on behalf of a covered entity or group of covered entities in exchange for payment for its services by a pharmacy benefits manager or pharmacy services administration organization. The term includes a pharmacy that generally dispenses outpatient prescriptions to covered individuals or dispenses particular types of prescriptions, provides pharmacy services to particular types of covered individuals or dispenses prescriptions in particular health care settings, including networks of specialty, institutional or long-term care facilities.

"Nonproprietary drug." As defined in section 2(7.1) of the act of September 27, 1961 (P.L.1700, No.699), known as the Pharmacy Act.

"Pharmacist." As defined in section 2(10) of the act of September 27, 1961 (P.L.1700, No.699), known as the Pharmacy Act.

"Pharmacy." As defined in section 2(12) of the act of September 27, 1961 (P.L.1700, No.699), known as the Pharmacy Act.

"Pharmacy audit." An audit, conducted on-site by or on behalf of an auditing entity of any records of a pharmacy for prescription or nonproprietary drugs dispensed by a pharmacy to a covered individual.

"Pharmacy benefits management." The performance of any of the following:

(1) The procurement of prescription drugs at a negotiated contracted rate for dispensation within this Commonwealth to covered individuals.

(2) The administration or management of prescription drug benefits provided by a covered entity for the benefit of covered individuals.

(3) The administration of pharmacy benefits, including:

(i) Operating a mail-service pharmacy.

(ii) Claims processing.

(iii) Managing a retail pharmacy network.

(iv) Paying claims to a pharmacy for prescription drugs dispensed to covered individuals via retail or mail-order pharmacy.

(v) Developing and managing a clinical formulary, including utilization management and quality assurance programs.

(vi) Rebate contracting and administration.

(vii) Managing a patient compliance, therapeutic intervention and generic substitution program.

(viii) Operating a disease management program.

(ix) Setting pharmacy reimbursement pricing and methodologies, including maximum allowable cost, and determining single or multiple source drugs.

"Pharmacy benefits manager" or "PBM." A person, business or other entity that performs pharmacy benefits management for covered entities.

"Pharmacy record." Any record stored electronically or as a hard copy by a pharmacy that relates to the provision of prescription or nonproprietary drugs or pharmacy services or other component of pharmacist care that is included in the practice of pharmacy.

"Pharmacy Services Administration Organization" or "PSAO." Any entity that contracts with a pharmacy to assist with third-party payer interactions and that may provide a variety of other administrative services, including contracting with PBMs on behalf of pharmacies and managing pharmacies' claims payments from third-party payers.

"Rare medical condition." A disease or condition that affects fewer than 200,000 individuals in the United States or approximately 1 in 1,500 individuals worldwide. (Def. added July 17, 2024, P.L.852, No.77)

"Retail pharmacy." A pharmacy where prescriptions are able to be dispensed to covered individuals on the premises of the pharmacy. (Def. added July 17, 2024, P.L.852, No.77)

"Specialty drug." Either of the following:

(1) A prescription drug prescribed to a covered individual with a cost that meets or exceeds the cost of a drug on the specialty tier of Medicare Part D under 42 CFR 423.104(d)(2)(iv) (relating to requirements related to qualified prescription drug coverage) and meets three or more of the following criteria:

(i) The drug requires specialized product handling or administration by the dispensing pharmacy.

(ii) The drug requires specialized clinical care, including, but not limited to, frequent dosing adjustments to the prescription drug, clinical monitoring or expanded patient service, intensive patient counseling and ongoing clinical support, such as individualized disease or therapy management to support patient outcomes for a covered individual.

(iii) The drug is prescribed for a covered individual with a rare medical condition, complex or chronic medical condition or life-threatening medical condition.

(iv) The prescription drug has a limited or exclusive distribution and is not typically stocked or dispensed by a retail pharmacy.

(2) A prescription drug that is prescribed to a covered individual and that is listed as a specialty drug on the medical assistance fee-for-service specialty pharmacy drug list.

(Def. added July 17, 2024, P.L.852, No.77)

"Specialty pharmacy." A pharmacy that has been nationally accredited by an independent third party to dispense specialty drugs. (Def. added July 17, 2024, P.L.852, No.77)

"Spread pricing." A model of prescription drug pricing in which the PBM charges a health benefit plan or health insurer a contracted price for prescription drugs and the contracted price for the prescription drugs differs from the amount the PBM directly or indirectly pays the pharmacist or pharmacy for prescription drugs and related pharmacist services. (Def. added July 17, 2024, P.L.852, No.77)

Section 104. Regulations.

Except as provided for in Chapter 10, the department may promulgate regulations necessary for the administration of this act.

(104 added July 17, 2024, P.L.852, No.77)

CHAPTER 3

PHARMACY AUDITS

Section 301. Procedures for conducting pharmacy audits.

(a) Procedure.--An entity conducting a pharmacy audit under this chapter shall conform to the following rules:

(1) Except as otherwise provided by Federal or State law, an auditing entity conducting a pharmacy audit may have access to a pharmacy's previous audit report only if the report was prepared by that auditing entity.

(2) Information collected during a pharmacy audit shall be confidential by law, except that the auditing entity conducting the pharmacy audit may share the information with the pharmacy benefits manager and the covered entity for which a pharmacy audit is being conducted.

(3) The auditing entity conducting a pharmacy audit may not solely compensate an employee or contractor with which an auditing entity contracts to conduct a pharmacy audit, solely based on the amount claimed or the actual amount recouped by the pharmacy being audited.

(4) The auditing entity shall provide the pharmacy being audited with at least 14 calendar days' prior written notice before conducting a pharmacy audit, unless both parties agree otherwise. If a delay is requested by the pharmacy, the pharmacy shall provide notice to the PBM within 72 hours of receiving notice of the audit.

(5) The auditing entity may not initiate or schedule a pharmacy audit during the first five business days of any month for a pharmacy that averages in excess of 600 prescriptions filled per week, without the express consent of the pharmacy.

(6) The auditing entity shall accept paper or electronic signature logs that document the delivery of prescription or nonproprietary drugs and pharmacist services to a health plan beneficiary or the beneficiary's caregiver or guardian.

(7) The auditing entity shall provide to the representative of the pharmacy, prior to leaving the pharmacy at the conclusion of the on-site portion of the pharmacy audit, a complete list of pharmacy records reviewed.

(8) A pharmacy audit that involves clinical judgment shall be conducted by or in consultation with a pharmacist.

(9) A pharmacy audit may not cover:

(i) a period of more than 24 months after the date a claim was submitted by the pharmacy to the pharmacy benefits manager or covered entity unless a longer period is required by law; or

(ii) more than 250 prescriptions, provided that a refill does not constitute a separate prescription for the purposes of this subparagraph.

(10) The auditing entity may not use extrapolation to calculate penalties or amounts to be charged back or recouped unless otherwise required by Federal requirements or Federal plans.

(11) The auditing entity may not include dispensing fees in the calculation of overpayments unless a prescription is considered a misfill. As used in this paragraph, "misfill" means a prescription that was not dispensed, a prescription error, a prescription where the prescriber denied the authorization request or a prescription where an extra dispensing fee was charged.

(12) A pharmacy may do any of the following when a pharmacy audit is performed:

(i) To validate the pharmacy record and delivery, a pharmacy may use authentic and verifiable statements or records, including, but not limited to, medication administration records of a nursing home, assisted living facility, hospital or health care practitioner with prescriptive authority.

(ii) To validate claims in connection with prescriptions or changes in prescriptions, or refills of prescription or nonproprietary drugs, a pharmacy may use any valid prescription, including, but not limited to, medication administration records, facsimiles, electronic prescriptions, electronically stored images of prescriptions, electronically created annotations or documented telephone calls from the prescribing health care practitioner or practitioner's agent. Documentation of an oral prescription order that has been verified by the prescribing health care practitioner shall meet the provisions of this subparagraph for the initial audit review.

(b) Written report.--An auditing entity shall provide the pharmacy with a written report of the pharmacy audit and comply with the following requirements:

(1) A preliminary pharmacy audit report must be delivered to the pharmacy or its corporate parent within 60 calendar days after the completion of the pharmacy audit. The preliminary report shall include contact information for the auditing entity who conducted the pharmacy audit and an appropriate and accessible point of contact, including telephone number, facsimile number, e-mail, and auditing firm, so that audit results, discrepancies and procedures can be reviewed. The preliminary pharmacy audit report shall include, but not be limited to, claim level information for any discrepancy found and total dollar amount of claims subject to recovery.

(2) A pharmacy shall be allowed 30 calendar days following receipt of the preliminary audit report to respond to the findings of the preliminary report.

(3) A final audit report shall be delivered to the pharmacy or its corporate parent not later than 60 calendar days after any responses from the pharmacy or corporate parent are received by the auditing entity. The auditing entity shall issue a final pharmacy audit report that takes into consideration any responses provided to the auditing entity by the pharmacy or corporate parent.

(4) The final audit report may be delivered electronically.

(5) A pharmacy may not be subject to a charge-back or recoupment for a clerical or recordkeeping error in a required document or record, including a typographical error, scrivener's error or computer error, unless the error resulted in overpayment to the pharmacy.

(6) An auditing entity conducting a pharmacy audit or person acting on behalf of the entity may not charge back or recoup or collect penalties from a pharmacy until the time period to file an appeal of a final pharmacy audit report has passed or the appeals process has been exhausted, whichever is later.

(7) If an identified discrepancy in a pharmacy audit exceeds $25,000, future payments to the pharmacy in excess of that amount may be withheld pending adjudication of an appeal.

(8) No interest shall accrue for any party during the audit period, beginning with the notice of the pharmacy audit and ending with the conclusion of the appeals process.

Section 302. Appeals process.

A pharmacy may appeal a final audit report in accordance with the procedures established by the entity conducting the pharmacy audit.

Section 303. Limitations.

(a) General rule.--The provisions of this chapter do not apply to an investigative audit of pharmacy records when:

(1) fraud, waste, abuse or other intentional misconduct is indicated by physical review or review of claims data or statements; or

(2) other investigative methods indicate a pharmacy is or has been engaged in criminal wrongdoing, fraud or other intentional or willful misrepresentation.

(b) Federal law.--This chapter does not supersede any audit requirements established by Federal law.

(c) Scrivener's error.--A scrivener's error made by a pharmacy not attributed to fraud, waste or abuse that is discovered during a pharmacy audit by the PBM shall result in the PBM recouping the dispensing fee for that particular transaction, not the entire amount for the medication received by the patient. ((c) added July 17, 2024, P.L.852, No.77)

Section 304. Regulations.

The department may promulgate regulations as necessary and appropriate to carry out this chapter.

CHAPTER 5

REGISTRATION

Section 501. PBM and auditing entity registration.

(a) General rule.--To conduct business in this Commonwealth, a PBM or auditing entity must register with the department. The department shall make an application form available on its publicly accessible Internet website that shall require:

(1) The identity, address and telephone number of the applicant.

(2) The name, business address and telephone number of the contact person for the applicant.

(3) When applicable, the Federal employer identification number for the applicant.

(a.1) PSAO registration.--To conduct business in this Commonwealth, a PSAO shall register with the department on an application form provided by the department. The form shall reflect the reporting requirements under section 704.1. Nothing under this subsection shall be construed as requiring a health insurer, health benefit plan or PBM to enter into a contract with a PSAO. ((a.1) added July 17, 2024, P.L.852, No.77)

(b) Term and fee.--

(1) The term of registration shall be two years from the date of issuance.

(2) The department shall set an initial application fee and a renewal application fee, which shall be submitted with an application for registration. An initial application fee shall be nonrefundable. A renewal application fee shall be returned if the renewal of the registration is not granted.

(3) The amount of the initial application fee and renewal application fee shall be sufficient to fund the department's duties in relation to its responsibilities under this chapter but may not exceed:

(i) $10,000 for a PBM or auditing entity.

(ii) $500 for a PSAO.

((b) amended July 17, 2024, P.L.852, No.77)

(c) Registration.--

(1) The department shall issue a registration, as appropriate, to an applicant when the department determines that the applicant has submitted a completed application and paid the required registration fee.

(2) The registration may be in paper or electronic form, shall be nontransferable and shall prominently list the expiration date of the registration.

(d) Duplicate registration.--

(1) A licensed insurer or a managed care plan with a certificate of authority shall comply with the standards and procedures of this act but shall not be required to separately register as either a PBM or auditing entity.

(2) A PBM that is registered under this chapter shall comply with the standards and procedures of this act but shall not be required to register separately as an auditing entity.

CHAPTER 6

PHARMACY BENEFITS MANAGER CONTRACTS

(Ch. added July 17, 2024, P.L. , No.77)

Compiler's Note: See section 14 of Act 77 of 2024 in the appendix to this act for special provisions relating to applicability.

Section 601. Contract provisions.

(a) General rule.--A PBM registered with the department and conducting business on behalf of a health insurer client in this Commonwealth may not:

(1) Reimburse a retail pharmacy an amount less than the amount that the PBM reimburses a PBM-affiliated retail pharmacy located in this Commonwealth for providing the same pharmacist services.

(2) Reimburse a federally qualified health center, health care facility or other entity participating in the program under section 340(b) of the Public Health Service Act (58 Stat. 682, 42 U.S.C. § 256(b)) an amount lesser than similar entities not participating in the program.

(3) Authorize the PBM to unilaterally alter the terms of a participation contract beyond the terms and conditions of the original contract agreed to by a PSAO or pharmacy with a PBM beyond the terms and conditions of the original contract agreed to by the pharmacy or PSAO with a PBM.

(4) Designate a prescription drug as a specialty drug or require a prescription drug to be dispensed exclusively at a specialty pharmacy unless it meets the criteria of a specialty drug under section 103.

(b) Rebates.--Beginning on the effective date of this section, a PBM shall pass through to the health benefit plan no less than 95% of any prescription drug manufacturer rebate obtained by the PBM on behalf of a health insurer client if the health benefit plan delegates negotiation of the rebate to the PBM.

(c) Contract information.--PBM contracts shall provide information to a pharmacist, pharmacy or PSAO pertaining to the schedule and total for any fee charged by the PBM for participation in the PBM's network.

(601 added July 17, 2024, P.L.852, No.77)

Section 602. Patient steering.

(a) Prohibitions.--A health benefit plan, health insurer or PBM contracting with a health benefit plan or health insurer may not:

(1) Require a covered individual, as a condition of payment or reimbursement, to purchase pharmacist services, including, but not limited to, prescription drugs, exclusively through a mail-order pharmacy or PBM retail pharmacy affiliate.

(2) Prohibit or limit a covered individual from selecting an in-network pharmacy or in-network pharmacist of the covered individual's choice if that pharmacy or pharmacist meets and agrees to the terms and conditions, including reimbursements, in the PBM's contract.

(3) Require a covered individual to use a PBM-affiliated retail pharmacy.

(4) Transfer a covered individual's prescriptions from an in-network pharmacy to another pharmacy unless requested by the covered individual.

(5) Use financial incentives, including, but not limited to, adjustments in cost sharing obligations of a covered individual, to the exclusive benefit of a PBM-affiliated retail pharmacy.

(6) Except as provided in subsection (b), auto-enroll a covered individual in mail-order pharmacy services.

(b) Construction.--Nothing in this section shall be construed:

(1) To prevent a PBM, health benefit plan or health insurer from requiring a covered individual to use an approved specialty pharmacy operating in the PBM's network.

(2) To prevent a health benefit plan, health insurer or PBM contracting with a health benefit plan or health insurer from auto-enrolling a covered individual in mail-order services for a maintenance medication, provided that:

(i) a covered individual may not be auto-enrolled for the first 90 days of a new maintenance medication; and

(ii) a covered individual shall have the ability to opt out of mail-order pharmacy services at any time.

(602 added July 17, 2024, P.L.852, No.77)

Section 603. Clawbacks prohibited.

(a) General rule.--A pharmacist, pharmacy intern or technician may not charge a patient an amount for a covered prescription drug that exceeds the lesser of:

(1) The net reimbursement paid to the pharmacy for the prescription drug by the health benefit plan, health insurer or PBM contracting with a health benefit plan or health insurer.

(2) The amount an individual would pay for the prescription drug if the prescription drug were purchased without coverage under a health benefit plan.

(b) Collection of difference in cost sharing.--A health benefit plan, health insurer or PBM contracting with a health benefit plan or health insurer may not collect from the member any difference in cost sharing the member pays to the pharmacy and the member's cost sharing defined in the member's benefit plan.

(603 added July 17, 2024, P.L.852, No.77)

Section 604. Network adequacy.

(a) General rule.--A PBM shall establish a reasonably adequate and accessible retail pharmacy network for the provision of prescription drugs under a health benefit plan that shall provide for convenient patient access to pharmacies within a reasonable distance from a patient's residence in accordance with the following requirements:

(1) The network may not be limited to affiliated pharmacies only.

(2) The network shall meet or exceed the requirements of 42 CFR 423.120(a) (relating to access to covered part D drugs) or a successor regulation. If a PBM fails to comply with the requirements, it shall not be considered a violation if the PBM contracts with all retail pharmacies within the network distance standards of the health benefit plan participants.

(b) Report requirement.--Beginning April 1, 2026, and annually thereafter, a PBM shall file with the department a network adequacy report, on a form prescribed by the department, describing the PBM network and the PBM network's accessibility in this Commonwealth. The reports shall be posted on the department's publicly accessible Internet website.

(604 added July 17, 2024, P.L.852, No.77)

CHAPTER 7

PBM COST TRANSPARENCY

REQUIREMENTS

Section 701. Multiple source generic list and reimbursement.

(a) General rule.--In order to place a particular drug on a multiple source generic list, a PBM shall, at a minimum, ensure that:

(1) the drug is listed as "A" or "B" rated in the most recent version of the Food and Drug Administration's "Approved Drug Products with Therapeutic Equivalence Evaluations," commonly known as the orange book, or "NR" or "NA" rated, or similar rating, by a nationally recognized reference;

(2) There are at least two therapeutically equivalent multiple source drugs or at least one generic drug available from only one manufacturer; and

(3) the drug is available for purchase by all pharmacies in this Commonwealth from national or regional wholesalers and is not obsolete or temporarily unavailable.

(b) Removal from listing.--A PBM must maintain a procedure to eliminate drugs from the list of drugs subject to multiple source drug pricing or modify the maximum allowable cost in a timely fashion.

(c) Substitutions.--A PBM may not penalize a pharmacist or pharmacy on audit if the pharmacist or pharmacy performs a generic substitution pursuant to the act of November 24, 1976 (P.L.1163, No.259), referred to as the Generic Equivalent Drug Law.

Section 702. Availability of multiple source generic list.

(a) General rule.--Upon each contract execution or renewal, a PBM shall, with respect to contracts between a PBM and a pharmacy, or its representative, including a PSAO:

(1) Include in the contract the sources utilized to determine multiple source drug pricing, including, if applicable, the maximum allowable cost or any successive pricing formula of the PBM.

(2) Update the pricing information every seven calendar days.

(3) Establish a reasonable process by which pharmacies have a method to access relevant or current maximum allowable cost pricing lists in effect and any successive pricing formulas in a timely fashion.

(b) Confidentiality provision.--Nothing in this section may prohibit a PBM from establishing a reasonable confidentiality provision with a pharmacy or its representative, including a PSAO.

Section 703. Multiple source drug pricing appeals process.

(a) Process to be established.--All contracts between a PBM or a pharmacy or, alternatively, a pharmacy's contracting agent, such a PSAO, shall include a process to appeal, investigate and resolve disputes regarding multiple source drug pricing. The contract provision establishing the process shall include the following:

(1) The right to appeal shall be limited to 14 calendar days following the initial claim.

(2) The appeal shall be investigated and resolved by the PBM through an internal process within 14 calendar days of receipt of the appeal by the PBM.

(3) A telephone number at which a pharmacy may contact the PBM and speak with an individual who is involved in the appeals process.

(b) Denial.--If a PBM denies an appeal, the PBM shall provide the reason for the denial and identify the national drug code of an equivalent drug that is available for purchase by network retail pharmacies in this Commonwealth from wholesalers at a price that is equal to or less than the maximum allowable cost for the appealed drug as determined by the PBM.

(c) Approval.--If a PBM grants an appeal, the PBM shall make the price correction, permit the reporting pharmacy to reverse and rebill the appealed claim and make the price correction effective for all similarly situated pharmacies from the date of the approved appeal.

Section 703.1. PBM transparency report required.

(a) General rule.--Beginning July 1, 2026, and annually thereafter, each registered PBM shall submit to the department a transparency report containing data for each health insurer client in this Commonwealth from the prior calendar year. The transparency report shall contain the following information:

(1) The aggregate amount of all rebates that the PBM received from all pharmaceutical manufacturers for all health insurer clients and for each health insurer client.

(2) The aggregate administrative fees that the PBM received from all manufacturers for all health insurer clients and for each health insurer client.

(3) The aggregate-retained rebates that the PBM received from all pharmaceutical manufacturers and did not pass through to health insurer clients.

(4) The highest, lowest and mean aggregate retained rebate percentage for all health insurer clients and for each health insurer client.

(5) For a PBM that controls or is affiliated with a pharmacy, a description of any differences between what the PBM reimburses or charges affiliated and nonaffiliated pharmacies.

(b) Publication.--Within 60 days of receipt, the department shall publish the transparency report under this section on the department's publicly accessible Internet website in a form that meets the following requirements:

(1) Does not disclose the name of a PBM.

(2) Does not directly or indirectly disclose the identity of a specific health insurer client or present information in a manner that can be extrapolated to identify a specific health insurer client.

(3) Does not list the price or prices charged for a specific drug or class of drugs.

(4) Does not specify the amount of any rebates provided for a specific drug or class of drug.

(c) Additional categories.--The department may, by regulation, direct PBMs to include additional categories for aggregated data from health insurer clients in the annual transparency report submitted under this section.

(d) Confidentiality.--

(1) The information submitted to the department in accordance with the transparency report required under subsection (a) shall be privileged and given confidential treatment and shall not be:

(i) subject to discovery or admissible as evidence in a private civil action;

(ii) subject to subpoena;

(iii) subject to access under the act of February 14, 2008 (P.L.6, No.3), known as the Right-to-Know Law; or

(iv) made public by the department or any other person without the prior written consent of the PBM, insurer or insurance group to which it pertains, except as provided in paragraph (3).

(2) The commissioner, the department, a person who receives information under subsection (a) while acting under the authority of the commissioner or department or a person with whom the information is shared under this chapter shall not be permitted or required to testify in a private civil action concerning confidential information in the transparency report.

(3) To assist in the performance of its regulatory duties, the department may:

(i) Use information submitted under this section in furtherance of a regulatory or legal action brought pursuant to the department's official duties.

(ii) Share information submitted under this section with the NAIC, regulatory or law enforcement officials of this Commonwealth or other jurisdictions, and third-party consultants, if, prior to receiving the transparency report information, the recipient demonstrates by written statement the necessary authority and intent to give confidential treatment to the information as required by this section.

(iii) Publish all or part of the information if, after giving the entity who would be affected thereby notice and opportunity to be heard, the department determines that the interest of the public will be served by the publication thereof.

(4) The sharing of information by the department under this section does not constitute a delegation of regulatory authority or rulemaking. The department shall be solely responsible for the administration, execution and enforcement of this chapter.

(5) The sharing of transparency report information with, to or by the department as authorized by this chapter does not constitute a waiver of any applicable privilege or claim of confidentiality.

(6) Information submitted under this section that is in the possession or control of the NAIC or a third-party consultant as provided under this section shall:

(i) be confidential and privileged;

(ii) be exempt from access under the Right-to-Know Law;

(iii) not be subject to subpoena; and

(iv) not be subject to discovery or admissible as evidence in a private civil action.

(703.1 added July 17, 2024, P.L.852, No.77)

Compiler's Note: See section 14 of Act 77 of 2024 in the appendix to this act for special provisions relating to applicability.

Section 704. Regulations (704 repealed July 17, 2024, P.L.852, No.77).

Section 704.1. PSAO reporting requirements.

A PSAO shall provide the following information to the department and each pharmacy that has contracted for services:

(1) Changes in the PSAO's ownership, including a parent company or subsidiary of the PSAO, no later than five days prior to the change in ownership of the PSAO, the parent company of a PSAO or a subsidiary of the PSAO.

(2) Whether the change in ownership includes a company or organization that provides pharmaceutical, prescription drug or device services.

(3) Whether the change in ownership includes a company that sells or manufacturers prescription drugs, biologics or medical devices.

(704.1 added July 17, 2024, P.L.852, No.77)

Section 705. Applicability.

This chapter shall apply to all contracts and agreements for pharmacy benefits management services executed or renewed on or after the effective date of this section.

CHAPTER 8

PACE AND PACENET PROGRAM PAYMENTS

Section 801. Definitions.

The following words and phrases when used in this chapter shall have the meanings given to them in this section unless the context clearly indicates otherwise:

"A-rated generic therapeutically equivalent drug." A drug product that the Commissioner of Food and Drugs of the United States Food and Drug Administration has approved as safe and effective and has determined to be therapeutically equivalent, as listed in "The Approved Drug Products with Therapeutic Equivalence Evaluations" (Food and Drug Administration "Orange Book"), with a specific "A" code designation only.

"Claimant." An eligible person who is enrolled in the program.

"Department." The Department of Aging of the Commonwealth.

"Less expensive." The lowest net cost to the program. The net cost shall include the amount paid by the Commonwealth to a pharmacy for a drug under a current retail pharmacy reimbursement formula less any discount or rebates, including those paid during the previous calendar quarter and inclusive of all dispensing fees.

"NADAC per unit." The current National Average Drug Acquisition Cost per unit.

"Prescription drug." All drugs requiring a prescription in this Commonwealth, insulin, insulin syringes and insulin needles. Experimental drugs or drugs prescribed for wrinkle removal or hair growth are prohibited.

"Program." The Pharmaceutical Assistance Contract for the Elderly (PACE) and the Pharmaceutical Assistance Contract for the Elderly Needs Enhancement Tier (PACENET) as established by the act of August 26, 1971 (P.L.351, No.91), known as the State Lottery Law.

"Provider." A pharmacy, dispensing physician or certified registered nurse practitioner enrolled as a provider in the program.

"Wholesale acquisition cost." The cost of a dispensed drug based upon the price published in a national drug pricing system in current use by the Department of Aging as the wholesale acquisition cost of a prescription drug in the most common package size.

Section 802. Program payment.

In addition to the requirements under section 509 of the act of August 26, 1971 (P.L.351, No.91), known as the State Lottery Law, the department shall administer the program in accordance with the following:

(1) If the NADAC per unit is available, the program payment shall be the lower of the following amounts:

(i) the NADAC per unit:

(A) with the addition of a professional dispensing fee of $13 per prescription; and

(B) the subtraction of the copayment; or

(ii) the pharmacy's usual and customary charge for the drug dispensed with the subtraction of the copayment.

(2) If the NADAC per unit is unavailable, the program payment shall be the lower of the following amounts:

(i) the wholesale acquisition cost plus 3.2%:

(A) with the addition of a professional dispensing fee of $13 per prescription; and

(B) the subtraction of the copayment; or

(ii) the pharmacy's usual and customary charge for the drug dispensed with the subtraction of the copayment.

Section 803. Generic drugs.

(a) General rule.--Notwithstanding any other statute or regulation, a brand name product shall be dispensed and not substituted with an A-rated generic therapeutically equivalent drug if it is less expensive to the program. If a less expensive A-rated generic therapeutically equivalent drug is available for dispensing to a claimant, the provider shall dispense the A-rated generic therapeutically equivalent drug to the claimant. The department shall reimburse providers based upon the most current listing of the NADAC per unit plus a professional dispensing fee of $13 per prescription. The department shall not reimburse providers for brand name products except in the following circumstances:

(1) There is no A-rated generic therapeutically equivalent drug available on the market. This paragraph does not apply to the lack of availability of an A-rated generic therapeutically equivalent drug in the providing pharmacy unless it can be shown to the department that the provider made reasonable attempts to obtain the A-rated generic therapeutically equivalent drug or that there was an unforeseeable demand and depletion of the supply of the A-rated generic therapeutically equivalent drug. In either case, the department shall reimburse the provider for the NADAC per unit plus a professional dispensing fee of $13 per prescription.

(2) An A-rated generic therapeutically equivalent drug is deemed by the department, in consultation with a utilization review committee, to have too narrow a therapeutic index for safe and effective dispensing in the community setting. The department shall notify providing pharmacies of A-rated generic therapeutically equivalent drugs that are identified pursuant to this paragraph on a regular basis.

(3) The Department of Health has determined that a drug shall not be recognized as an A-rated generic therapeutically equivalent drug for purpose of substitution under section 5(b) of the act of November 24, 1976 (P.L.1163, No.259), referred to as the Generic Equivalent Drug Law.

(4) At the time of dispensing, the provider has a prescription on which the brand name drug dispensed is billed to the program by the provider at a usual and customary charge which is equal to or less than the least expensive usual and customary charge of any A-rated generic therapeutically equivalent drug reasonably available on the market to the provider.

(5) The brand name drug is less expensive to the program.

(b) Generic not accepted.--If a claimant chooses not to accept the A-rated generic therapeutically equivalent drug required by subsection (a), the claimant shall be liable for the copayment and the NADAC per unit.

CHAPTER 9

ENFORCEMENTS

Section 901. Scope of enforcement authority.

(a) Scope.--The department may investigate and enforce the provisions of this act only insofar as the actions or inactions being investigated relate to prescription drug coverage under a health benefit plan.

(b) Remedy.--((b) deleted by amendment).

(b.1) Examination and access to records.--The following apply:

(1) (i) The department may order a PBM, a health insurer and a PBM's affiliates to produce records, books or other information as reasonably necessary to ascertain compliance with this act.

(ii) The department may retain an expert or experts as reasonably necessary to assist the department to conduct an analysis of PBM business practices under this paragraph. The reasonable and necessary costs for the expert services shall be paid by the PBM, payable within 30 days of the PBM's receipt of a bill for the services. Analysis under this section shall include:

(A) The impact of steering and spread pricing on the cost of prescription drugs to consumers in this Commonwealth and pharmacy access.

(B) The impact to consumers and pharmacies in this Commonwealth by requiring a health benefit plan or PBM contracting with a health benefit plan to reimburse a pharmacy utilizing the national average drug acquisition cost and a professional dispensing fee of $10.49.

(2) The department may examine or audit the books and records of a PBM, a health insurer and a PBM's affiliates to ascertain compliance with this act. The examination shall be conducted in accordance with Article IX of the act of May 17, 1921 (P.L.789, No.285), known as The Insurance Department Act of 1921.

(c) Review of specialty drugs.--The department shall establish an efficient process by which a pharmacy may refer designation of a prescription drug under a health benefit plan, by a PBM contracting with a health benefit plan, or a health insurer as a specialty drug which fails to meet the criteria under section 103. No later than 60 days following the effective date of this subsection, the department shall publish guidance to effectuate this subsection, including the list of prescription drugs classified as a specialty drug under the medical assistance fee-for-service program. The list under this subsection shall not be considered exclusive for the purposes of review by the department under this section. The department shall update guidance under this section to reflect changes in specialty drugs under the medical assistance fee-for-service program for each plan year.

(d) Penalties.--Upon the determination, after notice and hearing, that this act has been violated, the commissioner may impose the following penalties:

(1) Suspension or revocation of the licensee or registrant's license, authorization to operate or registration.

(2) Refusal to issue or renew a license, authorization to operate or registration.

(3) A cease and desist order.

(4) Order reimbursement to an insured, pharmacy or dispenser that has incurred a monetary loss as a result of a violation of this act.

(5) For each violation of this act that a licensee or registrant knew or reasonably should have known was a violation, a penalty of not more than $100,000, not to exceed an aggregate penalty of $1,000,000 in a single calendar year.

(6) For each violation of this act that a licensee or registrant did not know nor reasonably should have known was a violation, a penalty of not more than $50,000, not to exceed an aggregate penalty of $500,000 in a single calendar year.

(e) Additional remedies.--The enforcement remedies imposed under this section are in addition to any other remedies or penalties that may be imposed under any other applicable law of this Commonwealth, including the act of July 22, 1974 (P.L.589, No.205), known as the Unfair Insurance Practices Act. A violation of this act shall be deemed to be an unfair method of competition and an unfair or deceptive act or practice under the Unfair Insurance Practices Act.

(f) Administrative procedure.--The administrative provisions of this section shall be subject to 2 Pa.C.S. Ch. 5 Subch. A (relating to practice and procedure of Commonwealth agencies). A party against whom penalties are assessed in an administrative action may appeal to Commonwealth Court as provided in 2 Pa.C.S. Ch. 7 Subch. A (relating to judicial review of Commonwealth agency action).

(901 amended July 17, 2024, P.L.852, No.77)

CHAPTER 10

PHARMACY SERVICES

(Ch. added July 17, 2024, P.L.852, No.77)

Section 1001. Definitions.

The following words and phrases when used in this chapter shall have the meanings given to them in this section unless the context clearly indicates otherwise:

"Board." The State Board of Pharmacy.

"COVID-19" or "Coronavirus disease 2019." A highly contagious infectious disease caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).

"Direct and immediate personal supervision." As follows:

(1) Review by the pharmacist of the prescription or drug order prior to dispensing.

(2) Verification by the pharmacist of the final product.

(3) Immediate availability of the pharmacist on the premises to direct the work of the supervised individual and to respond to questions or problems.

"Licensee." An individual licensed by the board.

"Pharmacy Act." The act of September 27, 1961 (P.L.1700, No.699), known as the Pharmacy Act.

"Pharmacy technician." An individual who:

(1) Is required to be registered with the board as a pharmacy technician following the promulgation of final-form regulations under section 3 of the act of November 30, 2020 (P.L.1306, No.140), entitled "An act amending the act of September 27, 1961 (P.L.1700, No.699), entitled 'An act relating to the regulation of the practice of pharmacy, including the sales, use and distribution of drugs and devices at retail; and amending, revising, consolidating and repealing certain laws relating thereto,' further providing for definitions; and providing for pharmacy technician and pharmacy technician trainee registration, qualifications and supervision, for pharmacy technician data entry and for laboratory waiver."

(2) May assist in the practice of pharmacy under the direct and immediate personal supervision of a licensed pharmacist after meeting the requirements of this act, the Pharmacy Act and the regulations promulgated under this act or the Pharmacy Act. The term shall not include an individual performing clerical support with no direct interaction with prescription medication or ability to enter a prescription drug order.

"Practice of pharmacy." The following:

(1) The provision of health care services by a pharmacist, which includes:

(i) The interpretation, evaluation and implementation of medical orders for the provision of pharmacy services or prescription drug orders.

(ii) The delivery, dispensing or distribution of prescription drugs.

(iii) Participation in drug and device selection.

(iv) Drug administration.

(v) Drug regimen review.

(vi) Drug therapy management, including such services provided under the Medicare Prescription Drug, Improvement, and Modernization Act of 2003 (Public Law 108-173, 117 Stat. 2066).

(vii) Drug or drug-related research.

(viii) Compounding.

(ix) Proper and safe storage of drugs and devices.

(x) Management of drug therapy under section 9.3 of the Pharmacy Act, or, if in an institutional setting, consistent with the institution's assignment of clinical duties pursuant to a written agreement or protocol as specified in section 9.1 of the Pharmacy Act.

(xi) Maintaining proper records.

(xii) Patient counseling.

(xiii) Acts, services, operations or transactions necessary or incident to the provision of these health care services.

(2) The term shall not include the operations of a manufacturer or distributor as defined in The Controlled Substance, Drug, Device and Cosmetic Act.

"The Controlled Substance, Drug, Device and Cosmetic Act." The act of April 14, 1972 (P.L.233, No.64), known as The Controlled Substance, Drug, Device and Cosmetic Act, or the Controlled Substances Act (Public Law 91-513, 84 Stat. 1236).

(1001 added July 17, 2024, P.L.852, No.77)

Section 1002. Administration of injectable medications, biologicals and immunizations.

(a) General rule.--The board shall by regulation establish education and training standards and practice guidelines pursuant to which pharmacists shall be authorized to administer injectable medications, biologicals and immunizations to individuals eight years of age or older and influenza and COVID-19 immunizations by injectable or needle-free delivery methods to individuals five years of age or older. The standards and guidelines shall include, but not be limited to, the following:

(1) Satisfactory completion of an academic and practical curriculum approved by the board that includes the current guidelines and recommendations of the Centers for Disease Control and Prevention in the Public Health Service of the United States Department of Health and Human Services, the American Council on Pharmaceutical Education or a similar health authority or professional body and includes, but is not limited to, disease epidemiology, vaccine characteristics, injection technique, emergency response to adverse events and related topics.

(2) Maintenance of a current cardiopulmonary resuscitation (CPR) certificate acceptable to the board.

(3) That the administration of injectable medications, biologicals and immunizations be in accordance with a definitive set of treatment guidelines established by a physician and the Centers for Disease Control and Prevention, Advisory Committee on Immunization Practices guidelines or another competent authority approved by the board.

(4) That a minimum of two hours of the 30-hour requirement for continuing education for license renewal be dedicated to administering injectable medications, biologicals and immunizations.

(5) For individuals under 18 years of age, that parental consent be obtained prior to administration.

(6) Maintenance of a level of professional liability insurance coverage in the minimum amount of $1,000,000 per occurrence or claims made. Failure to maintain insurance coverage as required shall subject the licensees to disciplinary proceedings. The board shall accept as satisfactory evidence of insurance coverage any of the following:

(i) personally purchased liability insurance;

(ii) professional liability insurance coverage provided by the individual licensee's employer; or

(iii) similar insurance coverage acceptable to the board.

(7) Notification of the individual's primary care provider, if known, within 48 hours of administration.

(b) No delegation.--Except as provided under subsection (e), a pharmacist's authority to administer injectable medications, biologicals and immunizations shall not be delegated to any other individual. A pharmacy intern who has completed a course of education and training which meets the requirements of subsection (a)(1) and (2) and maintains liability insurance in the amounts specified under subsection (a)(6) may administer injectable medications, biologicals and immunizations, in keeping with the requirements under subsection (a)(3), to individuals who are eight years of age or older and influenza and COVID-19 immunizations by injectable or needle-free delivery methods to individuals five years of age or older only under the direct, immediate and personal supervision of a pharmacist holding the authority to administer injectable medications, biologicals and immunizations or a physician, physician assistant or certified registered nurse practitioner.

(c) Report of administration.--A supervising pharmacist shall report the administration of immunizations under this section to the immunization registry maintained by the Department of Health within 72 hours of immunization administration and to the individual's primary care provider in accordance with subsection (a)(7). Nothing in this subsection shall be construed to prohibit a supervising pharmacist from delegating the reporting of immunization administration to a pharmacy intern or technician.

(d) Information and referral.--A pharmacist, pharmacy intern or pharmacist technician who administers an influenza or COVID-19 immunization to an individual under 18 years of age shall inform the parent or adult caregiver of the importance of a well-child visit with a pediatrician or other licensed primary care provider and refer the patient as appropriate.

(e) Delegation of authority.--A pharmacist who holds the authority to administer injectable medications, biologicals and immunizations may delegate the authority to administer:

(1) Influenza and COVID-19 immunizations to a certified registered nurse practitioner, physician assistant, registered nurse or licensed practical nurse; or

(2) COVID-19 immunizations that are authorized or that are licensed by the United States Food and Drug Administration to individuals 13 years of age or older or influenza vaccinations that are recommended by the Advisory Committee on Immunization Practices to individuals 13 years of age or older to a pharmacy technician if:

(i) The pharmacy technician:

(A) Until the board promulgates final regulations implementing registration of pharmacy technicians, holds a national certification from the Pharmacy Technician Certification Board or the National Healthcareer Association; or

(B) After the board promulgates final regulations implementing registration of pharmacy technicians, is registered with the board.

(ii) The following conditions are met:

(A) The supervising qualified pharmacist is providing direct, immediate and personal supervision to the qualified pharmacy technician who is administering the immunizations or vaccinations.

(B) The qualified pharmacy technician has completed a practical training program that is approved by the Accreditation Council for Pharmacy Education and that includes hands-on injection technique and the recognition and treatment of emergency reactions to vaccines.

(C) The qualified pharmacy technician has a current certificate in basic cardiopulmonary resuscitation.

(D) The qualified pharmacy technician has obtained liability insurance as required under subsection (a)(6) through the qualified pharmacy technician's employer.

(E) Administration of a COVID-19 immunization or influenza vaccinations shall be in keeping with the requirements under subsection (a)(3).

(1002 added July 17, 2024, P.L.852, No.77)

Compiler's Note: See section 13 of Act 77 of 2024 in the appendix to this act for special provisions relating to continuation of prior law.

Section 1003. Clinical laboratory certificate.

(a) Certificate.--If a pharmacy holds a valid certificate of waiver issued by the Centers for Medicare and Medicaid Services, a pharmacy or pharmacist may order and perform laboratory examinations and procedures for COVID-19, influenza, respiratory syncytial virus and streptococcal infections authorized or approved by the United States Food and Drug Administration under the Clinical Laboratory Improvement Amendments of 1988 (Public Law 100-578, 102 Stat. 2903) and shall be exempt from the requirements under section 3 of the act of September 26, 1951 (P.L.1539, No.389), known as The Clinical Laboratory Act.

(b) Designation.--A pharmacist may designate the administration of a test under subsection (a) to a pharmacy intern or pharmacy technician if the designation by the pharmacist to a pharmacy intern or pharmacy technician and the administration of the test is in keeping with nationally recognized clinical practice guidelines that have not been disapproved by the Department of Health through transmission to the Legislative Reference Bureau for publication in the next available issue of the Pennsylvania Bulletin.

(1003 added July 17, 2024, P.L.852, No.77)

Section 1004. Report on pharmacy-administered vaccines.

(a) Report.--The Department of Health shall, in consultation with the board, report to the President pro tempore of the Senate, the Majority Leader and the Minority Leader of the Senate, the Speaker of the House of Representatives and the Majority Leader and the Minority Leader of the House of Representatives information concerning pharmacist activities authorized under this chapter, including:

(1) The number of injectable medications, biologicals and immunizations administered to individuals under 18 years of age broken down by age.

(2) The number of injectable medications, biologicals and immunizations administered to individuals under 18 years of age broken down by type of injectable medications, biologicals and immunizations.

(3) Subject to information being made available, an assessment on whether there is a change in the number of well visits for children with their primary pediatric care provider attributable pharmacist services authorized under this chapter.

(4) Beginning from the effective date of this section, changes in the pharmacy immunization rates for individuals under 18 years of age.

(b) Scope of report.--The Department of Health shall review data available for injectable medications, biologicals and immunizations administered by a pharmacist, pharmacy intern or technician in this Commonwealth. The Department of Health shall also review data available from other state governments which have authorized pharmacists to provide similar pharmacy services as authorized under this chapter.

(c) Timing of report.--The Department of Health shall report its findings no later than five years following the effective date of this subsection and include recommendations for changes in the laws of this Commonwealth.

(d) Publication.--Upon completion of the report and transmission of the report under subsection (a), the Department of Health shall publish the findings on the Department of Health's publicly accessible Internet website.

(1004 added July 17, 2024, P.L.852, No.77)

CHAPTER 11

MISCELLANEOUS PROVISIONS

Section 1101. Repeals.

Repeals are as follows:

(1) The General Assembly declares that the repeals under paragraph (2) are necessary to effectuate Chapter 8.

(2) Sections 509(6) and 510(a) and (b) of the act of August 26, 1971 (P.L.351, No.91), known as the State Lottery Law, are repealed.

Section 1102. Effective date.

This act shall take effect as follows:

(1) The following provisions shall take effect immediately:

(i) This chapter.

(ii) Chapter 8.

(2) Chapters 5 and 9 shall take effect in 90 days.

(3) The remainder of this act shall take effect in 180 days.

APPENDIX

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Supplementary Provisions of Amendatory Statutes

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2024, July 17, P.L. , NO.77

Section 13. The addition of section 1002 of the act is a continuation of sections 9.2 and 9.5 of the act of September 27, 1961 (P.L.1700, No.699), known as the Pharmacy Act. Except as otherwise provided in section 1002 of the act, all activities initiated under sections 9.2 and 9.5 of the Pharmacy Act shall continue and remain in full force and effect and may be completed under section 1002 of the act. Orders, regulations, rules and decisions which were made under sections 9.2 and 9.5 of the Pharmacy Act and which are in effect on the effective date of section 12(2) of this act shall remain in full force and effect until revoked, vacated or modified under section 1002 of the act. Contracts, obligations and collective bargaining agreements entered into under sections 9.2 and 9.5 of the Pharmacy Act are not affected nor impaired by the repeal of sections 9.2 and 9.5 of the Pharmacy Act.

Section 14. The following shall apply:

(1) The addition of Chapter 6 and section 703.1 of the act shall apply to a contract issued, renewed or amended after the effective date of this section.

(2) The following shall apply:

(i) For a health insurance policy for which either rates or forms are required to be filed with the Federal Government or the Insurance Department, this act shall apply to the health insurance policy for which a form or rate is first approved on or after the effective date of this paragraph.

(ii) For a health insurance policy for which neither rates nor forms are required to be filed with the Federal Government or the Insurance Department, this act shall apply to the health insurance policy issued or renewed on or after 180 days after the effective date of this paragraph.

Compiler's Note: Act 77 amended, added or repealed the title, sections 101, 102, 104, 303, 501, Chapter 6, sections 703.1, 704, 704.1, 901 and Chapter 10 of the act.