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3. A pharmacy that dispenses insulin under subd. 2. may submit to the
20manufacturer, or the manufacturer's vendor, a claim for payment that is in
21accordance with the national council for prescription drug programs' standards for
22electronic claims processing, except that no claim may be submitted if the
23manufacturer agrees to send the pharmacy a replacement of the same insulin in the
24amount dispensed. If the pharmacy submits an electronic claim, the manufacturer
1or vendor shall reimburse the pharmacy in an amount that covers the pharmacy's
2acquisition cost.
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4. A pharmacy that dispenses insulin under subd. 2. shall retain a copy of the
4application form described in subd. 1. a.
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(d)
Eligibility of certain individuals. An individual who has applied for public
6assistance under ch. 49 but for whom a determination of eligibility has not been made
7or whose coverage has not become effective or an individual who has an appeal
8pending under sub. (3) (c) 4. may access insulin under this subsection if the
9individual is in urgent need of insulin. To access a 30-day supply of insulin, the
10individual shall attest to the pharmacy that the individual is described in this
11paragraph and comply with par. (c) 1.
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12(3) Patient assistance program. (a)
Establishment of program. No later than
13July 1, 2024, each manufacturer shall establish a patient assistance program to
14make insulin available in accordance with this subsection to individuals who meet
15the eligibility requirements under par. (b). Under the patient assistance program,
16the manufacturer shall do all of the following:
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1. Provide the commissioner with information regarding the patient assistance
18program, including contact information for individuals to call for assistance in
19accessing the patient assistance program.
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2. Provide a hotline for individuals to call or access between 8 a.m. and 10 p.m.
21on weekdays and between 10 a.m. and 6 p.m. on Saturdays.
SB70,1604,2322
3. List the eligibility requirements under par. (b) on the manufacturer's
23website.
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4. Maintain the privacy of all information received from an individual applying
25for or participating in the patient assistance program and not sell, share, or
1disseminate the information unless required under this section or authorized, in
2writing, by the individual.
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(b)
Eligible individual. An individual shall be eligible to receive insulin under
4a patient assistance program if all of the following conditions are met:
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1. The individual is a resident of this state.
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2. The individual, or the individual's parent or legal guardian if the individual
7is under the age of 18, has a valid Wisconsin driver's license or state identification
8card.
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3. The individual has a valid insulin prescription.
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4. The family income of the individual does not exceed 400 percent of the
11poverty line as defined and revised annually under
42 USC 9902 (2) for a family the
12size of the individual's family.
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5. The individual is not receiving public assistance under ch. 49.
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6. The individual is not eligible to receive health care through a federally
15funded program or receive prescription drug benefits through the U.S. department
16of veterans affairs, except that this subdivision does not apply to an individual who
17is enrolled in a policy under Part D of Medicare under
42 USC 1395w-101 et seq. if
18the individual has spent at least $1,000 on prescription drugs in the current calendar
19year.
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7. The individual is not enrolled in prescription drug coverage through an
21individual or group health plan that limits the total cost sharing amount, including
22copayments, deductibles, and coinsurance, that an enrollee is required to pay for a
2330-day supply of insulin to no more than $75, regardless of the type or amount of
24insulin needed.
SB70,1606,9
1(c)
Application for patient assistance program. 1. An individual may apply to
2participate in a patient assistance program by filing an application with the
3manufacturer that established the patient assistance program, the individual's
4health care practitioner if the practitioner participates in the patient assistance
5program, or a navigator included on the list under sub. (8) (c).
A health care
6practitioner or navigator shall immediately submit the application to the
7manufacturer. Upon receipt of an application, the manufacturer shall determine the
8individual's eligibility under par. (b) and, except as provided in subd. 2., notify the
9individual of the determination no later than 10 days after receipt of the application.
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2. If necessary to determine the individual's eligibility under par. (b), the
11manufacturer may request additional information from an individual who has filed
12an application under subd. 1. no later than 5 days after receipt of the application.
13Upon receipt of the additional information, the manufacturer shall determine the
14individual's eligibility under par. (b) and notify the individual of the determination
15no later than 3 days after receipt of the requested information.
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3. Except as provided in subd. 5., if the manufacturer determines under subd.
171. or 2. that the individual is eligible for the patient assistance program, the
18manufacturer shall provide the individual with a statement of eligibility. The
19statement of eligibility shall be valid for 12 months and may be renewed upon a
20determination by the manufacturer that the individual continues to meet the
21eligibility requirements under par. (b).
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4. If the manufacturer determines under subd. 1. or 2. that the individual is not
23eligible for the patient assistance program, the manufacturer shall provide the
24reason for the determination in the notification under subd. 1. or 2. The individual
25may appeal the determination by filing an appeal with the commissioner that shall
1include all of the information provided to the manufacturer under subds. 1. and 2.
2The commissioner shall establish procedures for deciding appeals under this
3subdivision. The commissioner shall issue a decision no later than 10 days after the
4appeal is filed, and the commissioner's decision shall be final. If the commissioner
5determines that the individual meets the eligibility requirements under par. (b), the
6manufacturer shall provide the individual with the statement of eligibility described
7in subd. 3.
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5. In the case of an individual who has prescription drug coverage through an
9individual or group health plan,
if the manufacturer determines under subd. 1. or 2.
10that the individual is eligible for the patient assistance program but also determines
11that the individual's insulin needs are better addressed through the use of the
12manufacturer's copayment assistance program rather than the patient assistance
13program, the manufacturer shall inform the individual of the determination and
14provide the individual with the necessary coupons to submit to a pharmacy. The
15individual may not be required to pay more than the copayment amount specified in
16par. (d) 2.
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(d)
Provision of insulin under a patient assistance program. 1. Upon receipt
18from an individual of the eligibility statement described in par. (c) 3. and a valid
19insulin prescription, a pharmacy shall submit an order containing the name of the
20insulin and daily dosage amount to the manufacturer. The pharmacy shall include
21with the order the pharmacy's name, shipping address, office telephone number, fax
22number, email address, and contact name, as well as any days or times when
23deliveries are not accepted by the pharmacy.
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2. Upon receipt of an order meeting the requirements under subd. 1., the
25manufacturer shall send the pharmacy a 90-day supply of insulin, or lesser amount
1if requested in the order, at no charge to the individual or pharmacy. The pharmacy
2shall dispense the insulin to the individual associated with the order. The insulin
3shall be dispensed at no charge to the individual, except that the pharmacy may
4collect a copayment from the individual to cover the pharmacy's costs for processing
5and dispensing in an amount not to exceed $50 for each 90-day supply of insulin.
6The pharmacy may not seek reimbursement from the manufacturer or a 3rd-party
7payer.
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3. The pharmacy may submit a reorder to the manufacturer if the individual's
9eligibility statement described in par. (c) 3. has not expired. The reorder shall be
10treated as an order for purposes of subd. 2.
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4. Notwithstanding subds. 2. and 3., a manufacturer may send the insulin
12directly to the individual if the manufacturer provides a mail-order service option,
13in which case the pharmacy may not collect a copayment from the individual.
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14(4) Exceptions. (a) This section does not apply to a manufacturer that shows
15to the commissioner's satisfaction that the manufacturer's annual gross revenue
16from insulin sales in this state does not exceed $2,000,000.
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(b) A manufacturer may not be required to make an insulin product available
18under sub. (2) or (3) if the wholesale acquisition cost of the insulin product does not
19exceed $8, as adjusted annually based on the U.S. consumer price index for all urban
20consumers, U.S. city average, per milliliter or the applicable national council for
21prescription drug programs' plan billing unit.
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22(5) Confidentiality. All medical information solicited or obtained by any
23person under this section shall be subject to the applicable provisions of state law
24relating to confidentiality of medical information, including s. 610.70.
SB70,1609,6
1(6) Reimbursement prohibition. No person, including a manufacturer,
2pharmacy, pharmacist, or 3rd-party administrator, as part of participating in an
3urgent need safety net program or patient assistance program may request or seek,
4or cause another person to request or seek, any reimbursement or other
5compensation for which payment may be made in whole or in part under a federal
6health care program, as defined in
42 USC 1320a-7b (f).
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7(7) Reports. (a) Annually, no later than March 1, each manufacturer shall
8report to the commissioner all of the following information for the previous calendar
9year:
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1. The number of individuals who received insulin under the manufacturer's
11urgent need safety net program.
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2. The number of individuals who sought assistance under the manufacturer's
13patient assistance program and the number of individuals who were determined to
14be ineligible under sub. (3) (c) 4.
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3. The wholesale acquisition cost of the insulin provided by the manufacturer
16through the urgent need safety net program and patient assistance program.
SB70,1609,2017
(b) Annually, no later than April 1, the commissioner shall submit to the
18governor and the chief clerk of each house of the legislature, for distribution to the
19legislature under s. 13.172 (2), a report on the urgent need safety net programs and
20patient assistance programs that includes all of the following:
SB70,1609,2121
1. The information provided to the commissioner under par. (a).
SB70,1609,2322
2. The penalties assessed under sub. (9) during the previous calendar year,
23including the name of the manufacturer and amount of the penalty.
SB70,1610,3
24(8) Additional responsibilities of commissioner. (a)
Application form. The
25commissioner shall make the application form described in sub. (2) (c) 1. a. available
1on the office's website and shall make the form available to pharmacies and health
2care providers who prescribe or dispense insulin, hospital emergency departments,
3urgent care clinics, and community health clinics.
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(b)
Public outreach. 1. The commissioner shall conduct public outreach to
5create awareness of the urgent need safety net programs and patient assistance
6programs.
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2. The commissioner shall develop and make available on the office's website
8an information sheet that contains all of the following information:
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a. A description of how to access insulin through an urgent need safety net
10program.
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b. A description of how to access insulin through a patient assistance program.
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c. Information on how to contact a navigator for assistance in accessing insulin
13through an urgent need safety net program or patient assistance program.
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d. Information on how to contact the commissioner if a manufacturer
15determines that an individual is not eligible for a patient assistance program.
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e. A notification that an individual may contact the commissioner for more
17information or assistance in accessing ongoing affordable insulin options.
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(c)
Navigators. The commissioner shall develop a training program to provide
19navigators with information and the resources necessary to assist individuals in
20accessing appropriate long-term insulin options. The commissioner shall compile
21a list of navigators that have completed the training program and are available to
22assist individuals in accessing affordable insulin coverage options. The list shall be
23made available on the office's website and to pharmacies and health care
24practitioners who dispense and prescribe insulin.
SB70,1611,6
1(d)
Satisfaction surveys. 1. The commissioner shall develop and conduct a
2satisfaction survey of individuals who have accessed insulin through urgent need
3safety net programs and patient assistance programs. The survey shall ask whether
4the individual is still in need of a long-term solution for affordable insulin and shall
5include questions about the individual's satisfaction with all of the following, if
6applicable:
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a. Accessibility to urgent-need insulin.
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b. Adequacy of the information sheet and list of navigators received from the
9pharmacy.
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c. Helpfulness of a navigator.
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d. Ease of access in applying for a patient assistance program and receiving
12insulin from the pharmacy under the patient assistance program.
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2. The commissioner shall develop and conduct a satisfaction survey of
14pharmacies that have dispensed insulin through urgent need safety net programs
15and patient assistance programs. The survey shall include questions about the
16pharmacy's satisfaction with all of the following, if applicable:
SB70,1611,1817
a. Timeliness of reimbursement from manufacturers for insulin dispensed by
18the pharmacy under urgent need safety net programs.
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b. Ease in submitting insulin orders to manufacturers.
SB70,1611,2020
c. Timeliness of receiving insulin orders from manufacturers.
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3. The commissioner may contract with a nonprofit entity to develop and
22conduct the surveys under subds. 1. and 2. and to evaluate the survey results.
SB70,1611,2523
4. No later than July 1, 2026, the commissioner shall submit to the governor
24and the chief clerk of each house of the legislature, for distribution to the legislature
25under s. 13.172 (2), a report on the results of the surveys under subds. 1. and 2.
SB70,1612,5
1(9) Penalty. A manufacturer that violates this section may be required to
2forfeit not more than $200,000 per month of violation, with the maximum forfeiture
3increasing to $400,000 per month if the manufacturer continues to be in violation
4after 6 months and increasing to $600,000 per month if the manufacturer continues
5to be in violation after one year.
SB70,3091
6Section 3091
. 632.869 of the statutes is created to read:
SB70,1612,8
7632.869 Reimbursement to federal drug pricing program participants.
8 (
1) In this section:
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(a) “Covered entity” means an entity described in
42 USC 256b (a) (4) (A), (D),
10(E), (J), or (N) that participates in the federal drug pricing program under
42 USC
11256b, a pharmacy of the entity, or a pharmacy contracted with the entity to dispense
12drugs purchased through the federal drug pricing program under
42 USC 256b.
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(b) “Pharmacy benefit manager” has the meaning given in s. 632.865 (1) (c).
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14(2) No person, including a pharmacy benefit manager and 3rd-party payer,
15may do any of the following:
SB70,1612,1916
(a) Reimburse a covered entity for a drug that is subject to an agreement under
1742 USC 256b at a rate lower than that paid for the same drug to pharmacies that are
18not covered entities and have a similar prescription volume to that of the covered
19entity.
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(b) Assess a covered entity any fee, charge back, or other adjustment on the
21basis of the covered entity's participation in the federal drug pricing program under
2242 USC 256b.
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23(3) The commissioner may promulgate rules to implement this section and to
24establish a minimum reimbursement rate for covered entities and any other entity
25described under
42 USC 256b (a) (4).
SB70,3092
1Section
3092. 632.87 (4) of the statutes is amended to read:
SB70,1613,62
632.87
(4) No policy, plan or contract may exclude coverage for diagnosis and
3treatment of a condition or complaint by a licensed dentist
or dental therapist within
4the scope of the dentist's
or dental therapist's license, if the policy, plan or contract
5covers diagnosis and treatment of the condition or complaint by another health care
6provider, as defined in s. 146.81 (1) (a) to (p).
SB70,3093
7Section
3093
. 632.87 (7) of the statutes is created to read:
SB70,1613,88
632.87
(7) (a) In this subsection:
SB70,1613,99
1. “Health care provider” has the meaning given in s. 146.81 (1) (a) to (hp).
SB70,1613,1010
2. “Qualified treatment trainee” has the meaning given in s. DHS 35.03 (17m).
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(b) No policy, plan, or contract may exclude coverage for mental health or
12behavioral health treatment or services provided by a qualified treatment trainee
13within the scope of the qualified treatment trainee's education and training if the
14policy, plan, or contract covers the mental health or behavioral health treatment or
15services when provided by another health care provider.
SB70,3094
16Section
3094. 632.87 (8) of the statutes is created to read:
SB70,1613,1717
632.87
(8) (a) In this subsection:
SB70,1613,1818
1. “Health care provider” has the meaning given in s. 146.81 (1) (a) to (hp).
SB70,1613,2019
2. “Substance abuse counselor” means a substance abuse counselor certified
20under s. 440.88.
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(b) No policy, plan, or contract may exclude coverage for alcoholism or other
22drug abuse treatment or services provided by a substance abuse counselor within the
23scope of the substance abuse counselor's education and training if the policy, plan,
24or contract covers the alcoholism or other drug abuse treatment or services when
25provided by another health care provider.
SB70,3095
1Section
3095. 632.871 of the statutes is created to read:
SB70,1614,2
2632.871 Telehealth services. (1)
Definitions. In this section:
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(a) “Disability insurance policy” has the meaning given in s. 632.895 (1) (a).
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(b) “Self-insured health plan” means a self-insured health plan of the state or
5a county, city, village, town, or school district.
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(c) “Telehealth" means a practice of health care delivery, diagnosis,
7consultation, treatment, or transfer of medically relevant data by means of audio,
8video, or data communications that are used either during a patient visit or a
9consultation or are used to transfer medically relevant data about a patient.
10“Telehealth" does not include communications delivered solely by audio-only
11telephone, facsimile machine, or email unless specified otherwise by rule.
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12(2) Coverage denial prohibited. No disability insurance policy or self-insured
13health plan may deny coverage for a treatment or service provided through
14telehealth on the basis that the treatment or service is provided through telehealth
15if that treatment or service is covered by the disability insurance policy or
16self-insured health plan when provided in person. A disability insurance policy or
17self-insured health plan may limit coverage of treatments or services provided
18through telehealth to those treatments or services that are medically necessary.
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19(3) Certain limitations on telehealth prohibited. A disability insurance
20policy or self-insured health plan may not subject a treatment or service provided
21through telehealth for which coverage is required under sub. (2) to any of the
22following:
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(a) Any greater deductible, copayment, or coinsurance amount than would be
24applicable if the treatment or service is provided in person.
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1(b) Any policy or calendar year or lifetime benefit limit or other maximum
2limitation that is not imposed on other treatments or services covered by the
3disability insurance policy or self-insured health plan that are not provided through
4telehealth.
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(c) Prior authorization requirements that are not required for the same
6treatment or service when provided in person.
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(d) Unique location requirements.
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8(4) Disclosure of coverage of certain telehealth services. A disability
9insurance policy or self-insured health plan that covers a telehealth treatment or
10service that has no equivalent in-person treatment or service, such as remote patient
11monitoring, shall specify in policy or plan materials the coverage of that telehealth
12treatment or service.