88R23723 MPF-F
 
  By: Bonnen, Frank, Oliverson H.B. No. 4990
 
  Substitute the following for H.B. No. 4990:
 
  By:  Harless C.S.H.B. No. 4990
 
 
 
A BILL TO BE ENTITLED
 
AN ACT
  relating to the Texas Pharmaceutical Initiative; authorizing fees.
         BE IT ENACTED BY THE LEGISLATURE OF THE STATE OF TEXAS:
         SECTION 1.  Subtitle D, Title 10, Government Code, is
  amended by adding Chapter 2177 to read as follows:
  CHAPTER 2177.  TEXAS PHARMACEUTICAL INITIATIVE
         Sec. 2177.001.  DEFINITIONS. In this chapter:
               (1)  "Board" means the governing board of the
  initiative.
               (2)  "Fund" means the Texas Pharmaceutical Initiative
  fund.
               (3)  "Generic biological product" means a biological
  product approved pursuant to an application under Section 351(k),
  Public Health Service Act (42 U.S.C. Section 262(k)).
               (4)  "Generic drug" means a prescription drug approved
  pursuant to an application under Section 505(j), Federal Food,
  Drug, and Cosmetic Act (21 U.S.C. Section 355(j)).
               (5)  "Initiative" means the Texas Pharmaceutical
  Initiative established under this chapter.
         Sec. 2177.002.  TEXAS PHARMACEUTICAL INITIATIVE. (a)  The
  Texas Pharmaceutical Initiative is established to provide
  cost-effective access to prescription drugs and other medical
  supplies for:
               (1)  employees, dependents, and retirees of public
  higher education systems and institutions;
               (2)  Employees Retirement System of Texas members;
               (3)  Teacher Retirement System of Texas members;
               (4)  persons confined by the Texas Department of
  Criminal Justice or the Texas Juvenile Justice Department;
               (5)  recipients of medical assistance under Chapter 32,
  Human Resources Code; and
               (6)  enrollees of the child health plan program under
  Chapter 62, Health and Safety Code.
         (b)  A state entity that provides health benefit plan
  coverage to individuals described by Subsection (a) as the entity
  determines appropriate may elect to provide access to prescription
  drugs and other medical supplies under the initiative.
         Sec. 2177.003.  BOARD. (a) The initiative is governed by a
  board composed of:
               (1)  the executive commissioner of the Health and Human
  Services Commission or the executive commissioner's designee;
               (2)  the executive director of the Employees Retirement
  System of Texas or the executive director's designee;
               (3)  the executive director of the Teacher Retirement
  System of Texas or the executive director's designee;
               (4)  three members appointed by the governor;
               (5)  one member appointed by the governor from a list of
  three names submitted by the lieutenant governor;
               (6)  one member appointed by the governor from a list of
  three names submitted by the speaker of the house of
  representatives; and
               (7)  the chancellor of The University of Texas System,
  or the chancellor's designee, who serves in an ex-officio capacity.
         (b)  A vacancy on the board shall be filled in the same manner
  as the original appointment.
         (c)  The appointed board members serve staggered six-year
  terms.
         (d)  The governor shall designate the presiding officer of
  the board.
         (e)  A board member serves without compensation but may be
  reimbursed for travel and other actual and reasonable expenses
  incurred in the performance of the member's duties on the board.
         (f)  The board is administratively attached to the Health and
  Human Services Commission.
         Sec. 2177.004.  DUTIES OF BOARD. (a) The board shall:
               (1)  develop and implement the initiative and related
  programs established by this chapter;
               (2)  establish procedures and policies for the
  administration of the initiative;
               (3)  establish procedures to document compliance by
  board members and personnel with applicable laws governing
  conflicts of interest;
               (4)  ensure that a program or entity created under this
  chapter meets any applicable licensing or accreditation
  requirements under state or federal law; and
               (5)  recommend rules necessary to implement this
  chapter for adoption by the executive commissioner of the Health
  and Human Services Commission.
         (b)  To carry out the purposes of this chapter the board may:
               (1)  execute contracts and other instruments and
  conduct all activities the board determines necessary for those
  purposes;
               (2)  authorize one or more board members to execute
  contracts and other instruments on behalf of the board;
               (3)  establish a committee or other similar entity to
  exercise powers delegated by the board and exercise any other
  administrative duties or powers as the board considers necessary;
               (4)  employ an executive director and necessary
  personnel to provide administrative support; and
               (5)  award grants to public or private persons to
  implement the initiative.
         (c)  The board may refrain from establishing a program or
  entity under this chapter if the board determines that
  establishment is not feasible with current resources or considering
  other state-funded programs.
         (d)  A contract or agreement executed under this chapter must
  comply with Chapter 2254, if applicable.
         Sec. 2177.005.   PHARMACY BENEFIT MANAGER. (a) The board
  shall contract for a statewide pharmacy benefit manager, as
  provided by Subchapter H, Chapter 2158, to provide cost-effective
  prescription drugs through the establishment of a pharmacy network
  to state entities served by the initiative.
         (b)  The pharmacy benefit manager shall provide pricing
  transparency, a pass-through of all rebates and fees, and fair and
  equitable pricing to a pharmacy that participates in the pharmacy
  benefit manager's pharmacy network.
         (c)  The pharmacy benefit manager shall contract with
  appropriate persons to:
               (1)  provide an evidence-based benefit design, a prior
  authorization process, and a new drug review process; and
               (2)  partner with suppliers, pharmaceutical
  manufacturers, and group purchasing organizations for competitive
  acquisition of prescription drugs and medical supplies.
         Sec. 2177.006.  DISTRIBUTION OF PRESCRIPTION DRUGS AND
  MEDICAL SUPPLIES. (a) The board shall establish and implement a
  central service center and an associated network of satellite
  distribution facilities to provide prescription drugs and medical
  supplies to individuals described by Section 2177.002 for state
  entities that elect to participate in the initiative. The center
  must:
               (1)  be constructed to withstand extreme weather
  conditions, natural disasters, and power outages;
               (2)  be capable of providing disaster preparedness and
  response resources statewide; and
               (3)  include a mail order pharmacy and specialty
  pharmacy.
         (b)  The central service center may assess an inventory
  storage charge, transaction fees, or other fees on persons
  obtaining prescription drugs and medical supplies from the center
  to support the center's distribution and other operational costs,
  including overhead and margin.
         (c)  The mail order and specialty pharmacy established in the
  central service center may assess delivery and handling fees on
  persons receiving prescription drugs from the pharmacy.
         Sec. 2177.007.  PHARMACEUTICAL ADVANCED PREPARATION
  FACILITY. (a) The board shall establish a pharmaceutical advanced
  preparation facility to serve as an outsourcing facility in
  compliance with Section 503B, Federal Food, Drug, and Cosmetic Act
  (21 U.S.C. Section 353b), to:
               (1)  manufacture and provide compounded drugs;
               (2)  provide chimeric antigen receptor T-cell
  treatment and other gene therapies, including precision medicine;
  and
               (3)  provide advanced laboratories for quality
  control, preparation, and compounding of drugs in support of
  innovative therapeutics and drug research.
         (b)  The pharmaceutical advanced preparation facility shall
  be operated by an organization established by the board that is
  exempt from federal income taxation under Section 501(a), Internal
  Revenue Code of 1986, by being listed as an exempt entity under
  Section 501(c)(3) of that code.
         (c)  The pharmaceutical advanced preparation facility may
  charge fees to persons to whom the facility provides drugs,
  treatment, supplies, or other services to support the operational
  costs of the facility, including overhead and margin. 
         Sec. 2177.008.  ADVANCED HEALTH CARE COST AND CLAIMS
  ANALYTIC SERVICES. (a) The board shall contract with a person to
  provide advanced health care claims analytics software to support
  the programs and entities created by this chapter and to support
  population health research.
         (b)  The board shall develop criteria for the evaluation of
  applications or proposals submitted by a person seeking to contract
  with the board under this section.
         Sec. 2177.009.  GENERIC BIOLOGICAL PRODUCT AND GENERIC DRUG
  MANUFACTURING FACILITY. (a) The board may enter into an agreement
  with a person to establish a facility that manufactures generic
  biological products and generic drugs in compliance with any
  requirements of the federal Food and Drug Administration. In
  entering into the agreement, the board shall prioritize savings and
  access to affordable medications.
         (b)  The board shall develop criteria for the evaluation of
  applications or proposals submitted by a person seeking to contract
  with the board under this section.
         Sec. 2177.010.  CONFIDENTIALITY OF CERTAIN INFORMATION.  Any
  information received by the board, a program or entity created by
  this chapter, a state entity participating in the initiative, or a
  contractor or agent of the board that if directly or indirectly
  disclosed is likely to compromise the financial, competitive, or
  proprietary nature of the information, is confidential and not
  subject to disclosure under Chapter 552.
         Sec. 2177.011.  TEXAS PHARMACEUTICAL INITIATIVE FUND. (a)
  The Texas Pharmaceutical Initiative fund is created as a trust fund
  to be held by the comptroller outside the state treasury.
         (b)  The fund consists of:
               (1)  money from gifts, grants, and donations to the
  fund; 
               (2)  any additional legislative appropriations of
  money for the purposes of the fund; and
               (3)  interest, dividends, and other income of the fund.
         (c)  The board may only use money in the fund to carry out the
  purposes of this chapter.
         (d)  The board shall develop procedures for administration
  and approval of expenditures of the fund.
         Sec. 2177.012.  FUNDING. The board may accept gifts,
  grants, and donations from any public or private source for the
  purpose of carrying out this chapter.
         Sec. 2177.013.  ANNUAL REPORT. Not later than December 31 of
  each year, the board shall submit to the legislature a written
  report on:
               (1)  the activities and objectives of the initiative;
               (2)  any cost savings for state entities that
  participate in the initiative; and
               (3)  any recommendations for legislative or other
  action.
         SECTION 2.  This Act takes effect immediately if it receives
  a vote of two-thirds of all the members elected to each house, as
  provided by Section 39, Article III, Texas Constitution.  If this
  Act does not receive the vote necessary for immediate effect, this
  Act takes effect September 1, 2023.