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AB68-SSA1,1313,2120 563.22 (2) (c) All moneys received under this subsection shall be credited to the
21appropriation account under s. 20.505 (8) (jm) (jn).
AB68-SSA1,2943 22Section 2943. 563.80 (2m) of the statutes is amended to read:
AB68-SSA1,1313,2423 563.80 (2m) All moneys received under sub. (1) shall be credited to the
24appropriation account under s. 20.505 (8) (jm) (jn).
AB68-SSA1,2944 25Section 2944. 563.92 (2) of the statutes is amended to read:
AB68-SSA1,1314,10
1563.92 (2) The fee for a raffle license shall be $25 and shall be remitted with
2the application. A raffle license shall be valid for 12 months and may be renewed as
3provided in s. 563.98 (1g). The department shall issue the license within 30 days
4after the filing of a complete application if the applicant qualifies under s. 563.907
5and has not exceeded the limits of s. 563.91. The department shall notify the
6applicant within 15 days after it is filed if the raffle license application is incomplete
7or the application shall be considered complete. A complete license application that
8is not denied within 30 days after its filing shall be considered approved. All moneys
9received by the department under this subsection shall be credited to the
10appropriation account under s. 20.505 (8) (j) (jn).
AB68-SSA1,2945 11Section 2945. 563.98 (1g) of the statutes is amended to read:
AB68-SSA1,1314,1412 563.98 (1g) An organization licensed under this subchapter may renew the
13license by submitting a $25 renewal fee. All moneys received under this subsection
14shall be credited to the appropriation account under s. 20.505 (8) (j) (jn).
AB68-SSA1,2946 15Section 2946. 601.31 (1) (mv) of the statutes is created to read:
AB68-SSA1,1314,1816 601.31 (1) (mv) For initial licensure and renewal of licensure for pharmacy
17benefit management brokers and consultants, amounts set by the commissioner by
18rule.
AB68-SSA1,2947 19Section 2947. 601.31 (1) (nv) of the statutes is created to read:
AB68-SSA1,1314,2120 601.31 (1) (nv) For issuing or renewing a license to a pharmaceutical
21representative under s. 632.863, an amount to be set by the commissioner by rule.
AB68-SSA1,2948 22Section 2948 . 601.31 (1) (nw) of the statutes is created to read:
AB68-SSA1,1314,2523 601.31 (1) (nw) For issuing or renewing a license to a pharmacy services
24administrative organization under s. 632.864, an amount to be set by the
25commissioner by rule.
AB68-SSA1,2949
1Section 2949. 601.31 (1) (w) of the statutes is amended to read:
AB68-SSA1,1315,32 601.31 (1) (w) For initial issuance and for each annual renewal of a license as
3an administrator or pharmacy benefit manager under ch. 633, $100.
AB68-SSA1,2950 4Section 2950 . 601.41 (12) of the statutes is created to read:
AB68-SSA1,1315,95 601.41 (12) Employee misclassification outreach and education. The
6commissioner shall, on at least an annual basis, conduct outreach and education to
7persons subject to regulation under chs. 600 to 655 on how to identify the
8misclassification of employees as independent contractors and how to report
9suspected misclassifications to the appropriate federal and state agencies.
AB68-SSA1,2951 10Section 2951. 601.41 (13) of the statutes is created to read:
AB68-SSA1,1315,1611 601.41 (13) Value-based diabetes medication pilot project. The
12commissioner shall develop a pilot project to direct a pharmacy benefit manager, as
13defined in s. 632.865 (1) (c), and a pharmaceutical manufacturer to create a
14value-based, sole-source arrangement to reduce the costs of prescription medication
15used to treat diabetes. The commissioner may promulgate rules to implement this
16subsection.
AB68-SSA1,2952 17Section 2952 . 601.415 (3) of the statutes is repealed.
AB68-SSA1,2953 18Section 2953. 601.415 (14) of the statutes is created to read:
AB68-SSA1,1315,2419 601.415 (14) Patient pharmacy benefits tool. (a) From the appropriation
20under s. 20.145 (1) (a), beginning in the 2022-23 fiscal year, the office shall award
21grants in a total amount of up to $500,000 each fiscal year to health care providers
22to develop and implement a tool for prescribers to disclose the cost of prescription
23drugs for patients. The tool must be usable by physicians and other prescribers to
24determine the cost of prescription drugs for their patients.
AB68-SSA1,1316,2
1(b) Any health care provider that receives a grant under par. (a) shall contribute
2matching funds equal to at least 50 percent of the grant amount awarded.
AB68-SSA1,2954 3Section 2954 . 601.46 (3) (b) of the statutes is amended to read:
AB68-SSA1,1316,64 601.46 (3) (b) A general review of the insurance business in this state, including
5a report on emerging regulatory problems, developments and trends , including
6trends related to prescription drugs
;
AB68-SSA1,2955 7Section 2955. 601.575 of the statutes is created to read:
AB68-SSA1,1316,13 8601.575 Prescription drug importation program. (1) Importation
9program requirements.
The commissioner, in consultation with persons interested
10in the sale and pricing of prescription drugs and appropriate officials and agencies
11of the federal government, shall design and implement a prescription drug
12importation program for the benefit of residents of this state, that generates savings
13for residents, and that satisfies all of the following:
AB68-SSA1,1316,1614 (a) The commissioner shall designate a state agency to become a licensed
15wholesale distributor or to contract with a licensed wholesale distributor and shall
16seek federal certification and approval to import prescription drugs.
AB68-SSA1,1316,1917 (b) The prescription drug importation program under this section shall comply
18with relevant requirements of 21 USC 384, including safety and cost savings
19requirements.
AB68-SSA1,1316,2220 (c) The prescription drug importation program under this section shall import
21prescription drugs from Canadian suppliers regulated under any appropriate
22Canadian or provincial laws.
AB68-SSA1,1316,2523 (d) The prescription drug importation program under this section shall have
24a process to sample the purity, chemical composition, and potency of imported
25prescription drugs.
AB68-SSA1,1317,4
1(e) The prescription drug importation program under this section shall import
2only those prescription drugs for which importation creates substantial savings for
3residents of the state and only those prescription drugs that are not brand-name
4drugs and that have fewer than 4 competitor prescription drugs in the United States.
AB68-SSA1,1317,75 (f) The commissioner shall ensure that prescription drugs imported under the
6program under this section are not distributed, dispensed, or sold outside of the
7state.
AB68-SSA1,1317,98 (g) The prescription drug importation program under this section shall ensure
9all of the following:
AB68-SSA1,1317,1110 1. Participation by any pharmacy or health care provider in the program is
11voluntary.
AB68-SSA1,1317,1312 2. Any pharmacy or health care provider participating in the program has the
13appropriate license or other credential in this state.
AB68-SSA1,1317,1614 3. Any pharmacy or health care provider participating in the program charges
15a consumer or health plan the actual acquisition cost of the imported prescription
16drug that is dispensed.
AB68-SSA1,1317,2017 (h) The prescription drug importation program under this section shall ensure
18that a payment by a health plan or health insurance policy for a prescription drug
19imported under the program reimburses no more than the actual acquisition cost of
20the imported prescription drug that is dispensed.
AB68-SSA1,1317,2321 (i) The prescription drug importation program under this section shall ensure
22that any health plan or health insurance policy participating in the program does all
23of the following:
AB68-SSA1,1317,2524 1. Maintains a formulary and claims payment system with current information
25on prescription drugs imported under the program.
AB68-SSA1,1318,3
12. Bases cost-sharing amounts for participants or insureds under the plan or
2policy on no more than the actual acquisition cost of the prescription drug imported
3under the program that is dispensed to the participant or insured.
AB68-SSA1,1318,64 3. Demonstrates to the commissioner or a state agency designated by the
5commissioner how premiums under the policy or plan are affected by savings on
6prescription drugs imported under the program.
AB68-SSA1,1318,97 (j) Any wholesale distributor importing prescription drugs under the program
8under this section shall limit its profit margin to the amount established by the
9commissioner or a state agency designated by the commissioner.
AB68-SSA1,1318,1210 (k) The prescription drug importation program under this section may not
11import any generic prescription drug that would violate federal patent laws on
12branded products in this country.
AB68-SSA1,1318,1713 (L) The prescription drug importation program under this section shall comply
14to the extent practical and feasible, before the prescription drug to be imported comes
15into the possession of the state's wholesale distributor and fully after the prescription
16drug to be imported is in the possession of the state's wholesale distributor, with
17tracking and tracing requirements of 21 USC 360eee to 360eee-1.
AB68-SSA1,1318,2018 (m) The prescription drug importation program under this section shall
19establish a fee or other mechanism to finance the program that does not jeopardize
20significant savings to residents of the state.
AB68-SSA1,1318,2221 (n) The prescription drug importation program under this section shall have
22an audit function that ensures all of the following:
AB68-SSA1,1318,2523 1. The commissioner has a sound methodology to determine the most
24cost-effective prescription drugs to include in the importation program under this
25section.
AB68-SSA1,1319,2
12. The commissioner has a process in place to select Canadian suppliers that
2are high quality, high performing, and in full compliance with Canadian laws.
AB68-SSA1,1319,43 3. Prescription drugs imported under the program are pure, unadulterated,
4potent, and safe.
AB68-SSA1,1319,65 4. The prescription drug importation program is complying with the
6requirements of this subsection.
AB68-SSA1,1319,97 5. The prescription drug importation program under this section is adequately
8financed to support administrative functions of the program while generating
9significant cost savings to residents of the state.
AB68-SSA1,1319,1110 6. The prescription drug importation program under this section does not put
11residents of the state at a higher risk than if the program did not exist.
AB68-SSA1,1319,1312 7. The prescription drug importation program under this section provides and
13is projected to continue to provide substantial cost savings to residents of the state.
AB68-SSA1,1319,16 14(2) Anticompetitive behavior. The commissioner, in consultation with the
15attorney general, shall identify the potential for and monitor anticompetitive
16behavior in industries affected by a prescription drug importation program.
AB68-SSA1,1320,2 17(3) Approval of program design; certification. No later than the first day of
18the 7th month beginning after the effective date of this subsection .... [LRB inserts
19date], the commissioner shall submit to the joint committee on finance a report that
20includes the design of the prescription drug importation program in accordance with
21this section. The commissioner may not submit the proposed prescription drug
22importation program to the federal department of health and human services unless
23the joint committee on finance approves the proposed prescription drug
24implementation program. Within 14 days of the date of approval by the joint
25committee on finance of the proposed prescription drug importation program, the

1commissioner shall submit to the federal department of health and human services
2a request for certification of the approved prescription drug importation program.
AB68-SSA1,1320,10 3(4) Implementation of certified program. After the federal department of
4health and human services certifies the prescription drug importation program
5submitted under sub. (3), the commissioner shall begin implementation of the
6program, and the program shall be fully operational by 180 days after the date of
7certification by the federal department of health and human services. The
8commissioner shall do all of the following to implement the prescription drug
9importation program to the extent the action is in accordance with other state laws
10and the certification by the federal department of health and human services:
AB68-SSA1,1320,1311 (a) Become a licensed wholesale distributor, designate another state agency to
12become a licensed wholesale distributor, or contract with a licensed wholesale
13distributor.
AB68-SSA1,1320,1514 (b) Contract with one or more Canadian suppliers that meet the criteria in sub.
15(1) (c) and (n).
AB68-SSA1,1320,1916 (c) Create an outreach and marketing plan to communicate with and provide
17information to health plans and health insurance policies, employers, pharmacies,
18health care providers, and residents of the state on participating in the prescription
19drug importation program.
AB68-SSA1,1320,2220 (d) Develop and implement a registration process for health plans and health
21insurance policies, pharmacies, and health care providers interested in participating
22in the prescription drug importation program.
AB68-SSA1,1320,2423 (e) Create a publicly accessible source for listing prices of prescription drugs
24imported under the program.
AB68-SSA1,1321,3
1(f) Create, publicize, and implement a method of communication to promptly
2answer questions from and address the needs of persons affected by the
3implementation of the program before the program is fully operational.
AB68-SSA1,1321,54 (g) Establish the audit functions under sub. (1) (n) with a timeline to complete
5each audit function every 2 years.
AB68-SSA1,1321,86 (h) Conduct any other activities determined by the commissioner to be
7important to successful implementation of the prescription drug importation
8program under this section.
AB68-SSA1,1321,10 9(5) Report. By January 1 and July 1 of each year, the commissioner shall
10submit to the joint committee on finance a report including all of the following:
AB68-SSA1,1321,1211 (a) A list of prescription drugs included in the importation program under this
12section.
AB68-SSA1,1321,1513 (b) The number of pharmacies, health care providers, and health plans and
14health insurance policies participating in the prescription drug importation program
15under this section.
AB68-SSA1,1321,2016 (c) The estimated amount of savings to residents of the state, health plans and
17health insurance policies, and employers resulting from the implementation of the
18prescription drug importation program under this section reported from the date of
19the previous report under this subsection and from the date the program was fully
20operational.
AB68-SSA1,1321,2221 (d) Findings of any audit functions under sub. (1) (n) completed since the date
22of the previous report under this subsection.
AB68-SSA1,1321,24 23(6) Rulemaking. The commissioner may promulgate any rules necessary to
24implement this section.
AB68-SSA1,2956 25Section 2956. 601.59 of the statutes is created to read:
AB68-SSA1,1322,1
1601.59 State-based exchange. (1) Definitions. In this section:
AB68-SSA1,1322,22 (a) “Exchange” has the meaning given in 45 CFR 155.20.
AB68-SSA1,1322,53 (b) “State-based exchange on the federal platform” means an exchange that is
4described in and meets the requirements of 45 CFR 155.200 (f) and is approved by
5the federal secretary of health and human services under 45 CFR 155.106.
AB68-SSA1,1322,96 (c) “State-based exchange without the federal platform” means an exchange,
7other than one described in 45 CFR 155.200 (f), that performs all the functions
8described in 45 CFR 155.200 (a) and is approved by the federal secretary of health
9and human services under 45 CFR 155.106.
AB68-SSA1,1322,16 10(2) Establishment and operation of state-based exchange. The commissioner
11shall establish and operate an exchange that at first is a state-based exchange on
12the federal platform and then subsequently transitions to a state-based exchange
13without the federal platform. The commissioner shall develop procedures to address
14the transition from the state-based exchange on the federal platform to the
15state-based exchange without the federal platform, including the circumstances
16that shall be met in order for the transition to occur.
AB68-SSA1,1322,19 17(3) Agreement with federal government. The commissioner may enter into
18any agreement with the federal government necessary to facilitate the
19implementation of this section.
AB68-SSA1,1322,25 20(4) User fees. The commissioner shall impose a user fee, as authorized under
2145 CFR 155.160 (b) (1), on each insurer that offers a health plan through the
22state-based exchange on the federal platform or the state-based exchange without
23the federal platform. The user fee shall be applied at one of the following rates on
24the total monthly premiums charged by an insurer for each policy under the plan
25where enrollment is through the exchange:
AB68-SSA1,1323,2
1(a) For any plan year for which the commissioner operates a state-based
2exchange on the federal platform, the rate is 0.5 percent.
AB68-SSA1,1323,43 (b) For the first 2 plan years for which the commissioner operates a state-based
4exchange without the federal platform, the rate is 3 percent.
AB68-SSA1,1323,75 (c) Beginning with the 3rd plan year for which the commissioner operates a
6state-based exchange without the federal platform, the rate shall be set by the
7commissioner by rule.
AB68-SSA1,1323,9 8(5) Rules. The commissioner may promulgate rules necessary to implement
9this section.
AB68-SSA1,2957 10Section 2957. Subchapter VI (title) of chapter 601 [precedes 601.78] of the
11statutes is created to read:
AB68-SSA1,1323,1212 CHAPTER 601
AB68-SSA1,1323,1413 SUBCHAPTER VI
14 Prescription drug
AB68-SSA1,1323,1515 affordability review board
AB68-SSA1,2958 16Section 2958. 601.78 of the statutes is created to read:
AB68-SSA1,1323,17 17601.78 Definitions. In this subchapter:
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