AB748: Bill Text

For further information see the state fiscal estimate, which will be printed as an appendix to this bill.

The people of the state of Wisconsin, represented in senate and assembly, do enact as follows:

AB748,1 Section 1 . 20.005 (3) (schedule) of the statutes: at the appropriate place, insert the following amounts for the purposes indicated: - See PDF for table

AB748,2 Section 2 . 20.145 (1) (a) of the statutes is created to read:

AB748,7,5 20.145 (1) (a) State operations. The amounts in the schedule for general program operations.

AB748,3 Section 3 . 49.45 (18) (ac) of the statutes is amended to read:

AB748,8,9 49.45 (18) (ac) Except as provided in pars. (am) to (d), and subject to par. (ag), any person eligible for medical assistance under s. 49.46, 49.468, or 49.47, or for the benefits under s. 49.46 (2) (a) and (b) under s. 49.471, shall pay up to the maximum amounts allowable under 42 CFR 447.53 to 447.58 for purchases of services provided under s. 49.46 (2). The service provider shall collect the specified or allowable copayment, coinsurance, or deductible, unless the service provider determines that the cost of collecting the copayment, coinsurance, or deductible exceeds the amount to be collected. The department shall reduce payments to each provider by the amount of the specified or allowable copayment, coinsurance, or deductible. No provider may deny care or services because the recipient is unable to share costs, but an inability to share costs specified in this subsection does not relieve the recipient of liability for these costs.

AB748,4 Section 4 . 49.45 (18) (ag) of the statutes is repealed.

AB748,5 Section 5 . 49.45 (18) (b) 8. of the statutes is created to read:

AB748,8,12 49.45 (18) (b) 8. Prescription drugs.

AB748,6 Section 6 . 255.056 (2g) of the statutes is created to read:

AB748,8,19 255.056 (2g) The department may partner with out-of-state drug repository programs. The department may authorize a medical facility or pharmacy that elects to participate in the drug repository program to receive drugs or supplies from out of state, and the department may authorize an out-of-state entity that participates in a partner out-of-state drug repository program to receive drugs or supplies from Wisconsin.

AB748,7 Section 7 . 450.085 (3) of the statutes is created to read:

AB748,8,23 450.085 (3) An applicant for renewal of a license under s. 450.08 (2) (a) may count, for purposes of the continuing education requirement under sub. (1), up to 10 hours spent as a volunteer at a free and charitable clinic approved by the board.

AB748,8 Section 8 . 601.31 (1) (nv) of the statutes is created to read:

AB748,9,2 601.31 (1) (nv) For issuing or renewing a license as a pharmaceutical representative under s. 632.863, an amount to be set by the commissioner by rule.

AB748,9 Section 9 . 601.31 (1) (nw) of the statutes is created to read:

AB748,9,6 601.31 (1) (nw) For issuing or renewing a license as a pharmacy services administrative organization under s. 632.864, an amount to be set by the commissioner by rule.

AB748,10 Section 10 . 601.41 (13) of the statutes is created to read:

AB748,9,13 601.41 (13) Value-based diabetes medication pilot project. The commissioner shall develop a pilot project to direct a pharmacy benefit manager, as defined in s. 632.865 (1) (c), and a pharmaceutical manufacturer to create a value-based, sole-source arrangement to reduce the costs of prescription medication used to treat diabetes. The commissioner may promulgate rules to implement this subsection.

AB748,11 Section 11 . 601.415 (14) of the statutes is created to read:

AB748,9,20 601.415 (14) Patient pharmacy benefits tool. (a) From the appropriation under s. 20.145 (1) (a), beginning in the 2024-25 fiscal year, the office shall award grants in a total amount of up to $500,000 each fiscal year to health care providers to develop and implement a tool for prescribers to disclose the cost of prescription drugs for patients. The tool must be usable by physicians and other prescribers to determine the cost of prescription drugs for their patients.

AB748,9,22 (b) Any health care provider that receives a grant under par. (a) shall contribute matching funds equal to at least 50 percent of the grant amount awarded.

AB748,12 Section 12 . 601.575 of the statutes is created to read:

AB748,9,25 601.575 Prescription drug importation program. (1) Importation program requirements. The commissioner, in consultation with persons interested in the sale and pricing of prescription drugs and appropriate officials and agencies of the federal government, shall design and implement a prescription drug importation program for the benefit of residents of this state, that generates savings for residents, and that satisfies all of the following:

AB748,10,7 (a) The commissioner shall designate a state agency to become a licensed wholesale distributor or to contract with a licensed wholesale distributor and shall seek federal certification and approval to import prescription drugs.

AB748,10,9 (b) The program shall comply with relevant requirements of 21 USC 384, including safety and cost savings requirements.

AB748,10,11 (c) The program shall import prescription drugs from Canadian suppliers regulated under any appropriate Canadian or provincial laws.

AB748,10,13 (d) The program shall have a process to sample the purity, chemical composition, and potency of imported prescription drugs.

AB748,10,17 (e) The program shall import only those prescription drugs for which importation creates substantial savings for residents of this state and only those prescription drugs that are not brand-name drugs and that have fewer than 4 competitor prescription drugs in the United States.

AB748,10,19 (f) The commissioner shall ensure that prescription drugs imported under the program are not distributed, dispensed, or sold outside of this state.

AB748,10,20 (g) The program shall ensure all of the following:

AB748,10,22 1. Participation by any pharmacy or health care provider in the program is voluntary.

AB748,10,24 2. Any pharmacy or health care provider participating in the program has the appropriate license or other credential in this state.

AB748,11,3 3. Any pharmacy or health care provider participating in the program charges a consumer or health plan the actual acquisition cost of the imported prescription drug that is dispensed.

AB748,11,7 (h) The program shall ensure that a payment by a health plan or health insurance policy for a prescription drug imported under the program reimburses no more than the actual acquisition cost of the imported prescription drug that is dispensed.

AB748,11,9 (i) The program shall ensure that any health plan or health insurance policy participating in the program does all of the following:

AB748,11,11 1. Maintains a formulary and claims payment system with current information on prescription drugs imported under the program.

AB748,11,14 2. Bases cost-sharing amounts for participants or insureds under the plan or policy on no more than the actual acquisition cost of the prescription drug imported under the program that is dispensed to the participant or insured.

AB748,11,17 3. Demonstrates to the commissioner or a state agency designated by the commissioner how premiums under the plan or policy are affected by savings on prescription drugs imported under the program.

AB748,11,20 (j) Any wholesale distributor importing prescription drugs under the program shall limit its profit margin to the amount established by the commissioner or a state agency designated by the commissioner.

AB748,11,22 (k) The program may not import any generic prescription drug that would violate federal patent laws on branded products in the United States.

AB748,12,2 (L) The program shall comply with tracking and tracing requirements of 21 USC 360eee and 360eee-1, to the extent practical and feasible, before the prescription drug to be imported comes into the possession of this state's wholesale distributor and fully after the prescription drug to be imported is in the possession of this state's wholesale distributor.

AB748,12,4 (m) The program shall establish a fee or other mechanism to finance the program that does not jeopardize significant savings to residents of this state.

AB748,12,5 (n) The program shall have an audit function that ensures all of the following:

AB748,12,7 1. The commissioner has a sound methodology to determine the most cost-effective prescription drugs to include in the program.

AB748,12,9 2. The commissioner has a process in place to select Canadian suppliers that are high quality, high performing, and in full compliance with Canadian laws.

AB748,12,11 3. Prescription drugs imported under the program are pure, unadulterated, potent, and safe.

AB748,12,12 4. The program is complying with the requirements of this subsection.

AB748,12,14 5. The program is adequately financed to support administrative functions of the program while generating significant cost savings to residents of this state.

AB748,12,16 6. The program does not put residents of this state at a higher risk than if the program did not exist.

AB748,12,18 7. The program provides and is projected to continue to provide substantial cost savings to residents of this state.

AB748,12,21 (2) Anticompetitive behavior. The commissioner, in consultation with the attorney general, shall identify the potential for and monitor anticompetitive behavior in industries affected by a prescription drug importation program.

AB748,13,6 (3) Approval of program design; certification. No later than the first day of the 7th month beginning after the effective date of this subsection .... [LRB inserts date], the commissioner shall submit to the joint committee on finance a report that includes the design of the prescription drug importation program in accordance with this section. The commissioner may not submit the proposed program to the federal department of health and human services unless the joint committee on finance approves the proposed program. Within 14 days of the date of approval by the joint committee on finance of the proposed program, the commissioner shall submit to the federal department of health and human services a request for certification of the approved program.

AB748,13,14 (4) Implementation of certified program. After the federal department of health and human services certifies the prescription drug importation program submitted under sub. (3), the commissioner shall begin implementation of the program, and the program shall be fully operational by 180 days after the date of certification by the federal department of health and human services. The commissioner shall do all of the following to implement the program to the extent the action is in accordance with other state laws and the certification by the federal department of health and human services:

AB748,13,17 (a) Become a licensed wholesale distributor, designate another state agency to become a licensed wholesale distributor, or contract with a licensed wholesale distributor.

AB748,13,19 (b) Contract with one or more Canadian suppliers that meet the criteria in sub. (1) (c) and (n).

AB748,13,22 (c) Create an outreach and marketing plan to communicate with and provide information to health plans and health insurance policies, employers, pharmacies, health care providers, and residents of this state on participating in the program.

AB748,13,25 (d) Develop and implement a registration process for health plans and health insurance policies, pharmacies, and health care providers interested in participating in the program.

AB748,14,2 (e) Create a publicly accessible source for listing prices of prescription drugs imported under the program.

AB748,14,5 (f) Create, publicize, and implement a method of communication to promptly answer questions from and address the needs of persons affected by the implementation of the program before the program is fully operational.

AB748,14,7 (g) Establish the audit functions under sub. (1) (n) with a timeline to complete each audit function every 2 years.

AB748,14,9 (h) Conduct any other activities determined by the commissioner to be important to successful implementation of the program.

AB748,14,11 (5) Report. By January 1 and July 1 of each year, the commissioner shall submit to the joint committee on finance a report including all of the following:

AB748,14,13 (a) A list of prescription drugs included in the prescription drug importation program under this section.

AB748,14,16 (b) The number of pharmacies, health care providers, and health plans and health insurance policies participating in the prescription drug importation program under this section.

AB748,14,21 (c) The estimated amount of savings to residents of this state, health plans and health insurance policies, and employers resulting from the implementation of the prescription drug importation program under this section reported from the date of the previous report under this subsection and from the date the program was fully operational.

AB748,14,23 (d) Findings of any audit functions under sub. (1) (n) completed since the date of the previous report under this subsection.

AB748,14,25 (6) Rulemaking. The commissioner may promulgate any rules necessary to implement this section.

AB748,13 Section 13 . 609.83 of the statutes is amended to read:

AB748,15,4 609.83 Coverage of drugs and devices. Limited service health organizations, preferred provider plans, and defined network plans are subject to ss. 632.853, 632.861, and 632.895 (6) (b), (16t) , and (16v).

AB748,14 Section 14 . 632.863 of the statutes is created to read:

AB748,15,6 632.863 Pharmaceutical representatives. (1) Definitions. In this section:

AB748,15,9 (a) “Health care professional” means a physician or other health care practitioner who is licensed to provide health care services or to prescribe pharmaceutical or biologic products.

AB748,15,11 (b) “Pharmaceutical” means a medication that may legally be dispensed only with a valid prescription from a health care professional.

AB748,15,14 (c) “Pharmaceutical representative” means an individual who markets or promotes pharmaceuticals to health care professionals on behalf of a pharmaceutical manufacturer for compensation.

AB748,15,18 (d) “Wholesale acquisition cost” means the most recently reported manufacturer list or catalog price for a brand-name or generic drug available to wholesalers or direct purchasers in the United States, before application of discounts, rebates, or reductions in price.

AB748,15,24 (2) Licensure. (a) No individual may act as a pharmaceutical representative in this state without being licensed by the commissioner as a pharmaceutical representative under this section. In order to obtain a license, the individual shall apply to the commissioner in the form and manner prescribed by the commissioner. The term of a license issued under this paragraph is one year and is renewable. The application to obtain or renew a license shall include all of the following information:

AB748,16,2 1. The applicant's full name, residence address and telephone number, and business address and telephone number.

AB748,16,3 2. A description of the type of work in which the applicant will engage.

AB748,16,4 3. The fee under s. 601.31 (1) (nv).

AB748,16,6 4. An attestation that the applicant meets the professional education requirements under sub. (3).

AB748,16,7 5. Proof that the applicant has paid any assessed penalties and fees.

AB748,16,8 6. Any other information required by the commissioner.

AB748,16,14 (b) The pharmaceutical representative licensed under par. (a) shall report, in writing, to the commissioner any change to the information submitted on an application under par. (a) or any material change to the pharmaceutical representative's business operations or to any information provided under this section. The pharmaceutical representative shall make the report no later than 4 business days after the change or material change occurs.

AB748,16,17 (c) A pharmaceutical representative licensed under par. (a) shall display the pharmaceutical representative's license during each visit with a health care professional.

AB748,16,22 (3) Professional education requirements. (a) In order to become initially licensed under sub. (2) (a), a pharmaceutical representative shall complete a professional education course as determined by the commissioner. A pharmaceutical representative shall, upon request, provide the commissioner with proof of the coursework's completion.

AB748,17,2 (b) In order to renew a license under sub. (2) (a), a pharmaceutical representative shall complete a minimum of 5 hours of continuing professional education courses. A pharmaceutical representative shall, upon request, provide the commissioner with proof of the coursework's completion.