Bill Text: MI SB0429 | 2011-2012 | 96th Legislature | Engrossed


Bill Title: Insurance; health; standardized prior authorization form for prescription drugs; require. Amends 1956 PA 218 (MCL 500.100 - 500.8302) by adding sec. 2212c. TIE BAR WITH: SB 0430'11

Spectrum: Moderate Partisan Bill (Republican 8-2)

Status: (Engrossed - Dead) 2012-03-29 - Referred To Committee On Insurance [SB0429 Detail]

Download: Michigan-2011-SB0429-Engrossed.html

SB-0429, As Passed Senate, March 29, 2012

 

 

 

 

 

 

 

 

 

 

 

SUBSTITUTE FOR

 

SENATE BILL NO. 429

 

 

 

 

 

 

 

 

 

 

 

 

     A bill to amend 1956 PA 218, entitled

 

"The insurance code of 1956,"

 

(MCL 500.100 to 500.8302) by adding section 2212c.

 

THE PEOPLE OF THE STATE OF MICHIGAN ENACT:

 

     Sec. 2212c. (1) On or before January 1, 2013, the commissioner

 

shall develop a standard prior authorization methodology for use by

 

prescribers to request and receive prior authorization from an

 

insurer when a policy, certificate, or contract requires prior

 

authorization for prescription drug benefits. The commissioner

 

shall include in the standard prior authorization methodology the

 

ability for the prescriber to designate the prior authorization

 

request for expedited review. In order to designate a prior

 

authorization request for expedited review, the prescriber shall

 

certify that applying the 15-day standard review period may


 

seriously jeopardize the life or health of the patient or the

 

patient's ability to regain maximum function.

 

     (2) Within 30 days after the effective date of this section,

 

the commissioner shall appoint a workgroup, the members of which

 

shall represent insurers, prescribers, pharmacists, hospitals, and

 

other stakeholders in the development of a standard prior

 

authorization methodology. The workgroup shall assist in the

 

development of the standard prior authorization methodology under

 

subsection (1).

 

     (3) In developing the standard prior authorization methodology

 

under subsection (1), the commissioner shall hold 1 or more public

 

hearings to gather input from interested parties. In developing the

 

standard prior authorization methodology under subsection (1), the

 

commissioner and workgroup shall consider all of the following:

 

     (a) Existing and potential technologies that could be used to

 

transmit a standard prior authorization request.

 

     (b) The national standards pertaining to electronic prior

 

authorization developed by the national council for prescription

 

drug programs.

 

     (c) Any prior authorization forms and methodologies used in

 

pilot programs in this state.

 

     (d) Any prior authorization forms and methodologies developed

 

by the federal centers for medicare and medicaid services.

 

     (4) Beginning on the effective date of this section, an

 

insurer may specify in writing the materials and information

 

necessary to constitute a properly completed standard prior

 

authorization request when a policy, certificate, or contract


 

requires prior authorization for prescription drug benefits.

 

     (5) If the commissioner develops a paper form as the standard

 

prior authorization methodology under subsection (1), the paper

 

form shall meet all of the following requirements:

 

     (a) Consist of not more than 2 pages. However, an insurer may

 

request and require additional information beyond the 2-page

 

limitation of this subdivision, if that information is specified in

 

writing by the insurer under subsection (4). As used in this

 

subdivision, "additional information" includes, but is not limited

 

to, any of the following:

 

     (i) Patient clinical information including, but not limited to,

 

diagnosis, chart notes, lab information, and genetic tests.

 

     (ii) Information necessary for approval of the prior

 

authorization request under plan criteria.

 

     (iii) Drug specific information including, but not limited to,

 

medication history, duration of therapy, and treatment use.

 

     (b) Be electronically available.

 

     (c) Be electronically transmissible, including, but not

 

limited to, transmission by facsimile or similar device.

 

     (6) Beginning July 1, 2014, if an insurer uses a prior

 

authorization methodology that utilizes an internet webpage,

 

internet webpage portal, or similar electronic, internet, and web-

 

based system, the prior authorization methodology described in

 

subsection (5) does not apply. Subsections (4), (8), and (9) apply

 

to a prior authorization methodology that utilizes an internet

 

webpage, internet webpage portal, or similar electronic, internet,

 

and web-based system.


 

     (7) Beginning July 1, 2014, except as otherwise provided in

 

subsection (6), an insurer shall use the standard prior

 

authorization methodology developed under subsection (1) when a

 

policy, certificate, or contract requires prior authorization for

 

prescription drug benefits.

 

     (8) Beginning January 1, 2014, a prior authorization request

 

that has not been certified for expedited review by the prescriber

 

is considered to have been granted by the insurer if the insurer

 

fails to grant the request, deny the request, or require additional

 

information of the prescriber within 15 days after the date and

 

time of submission of a standard prior authorization request under

 

this section. If additional information is requested by an insurer,

 

a prior authorization request under this subsection is not

 

considered granted if the prescriber fails to submit the additional

 

information within 15 days after the date and time of the original

 

submission of a properly completed standard prior authorization

 

request under this section. If additional information is requested

 

by an insurer, a prior authorization request is considered to have

 

been granted by the insurer if the insurer fails to grant the

 

request, deny the request, or otherwise respond to the request of

 

the prescriber within 15 days after the date and time of submission

 

of the additional information. If additional information is

 

requested by an insurer, a prior authorization request under this

 

subsection is considered void if the prescriber fails to submit the

 

additional information within 21 days after the date and time of

 

the original submission of a properly completed standard prior

 

authorization request under this section.


 

     (9) Beginning January 1, 2014, a prior authorization request

 

that has been certified for expedited review by the prescriber is

 

considered to have been granted by the insurer if the insurer fails

 

to grant the request, deny the request, or require additional

 

information of the prescriber within 72 hours after the date and

 

time of submission of a standard prior authorization request under

 

this section. If additional information is requested by an insurer,

 

a prior authorization request under this subsection is not

 

considered granted if the prescriber fails to submit the additional

 

information within 72 hours after the date and time of the original

 

submission of a properly completed standard prior authorization

 

request under this section. If additional information is requested

 

by an insurer, a prior authorization request is considered to have

 

been granted by the insurer if the insurer fails to grant the

 

request, deny the request, or otherwise respond to the request of

 

the prescriber within 72 hours after the date and time of

 

submission of the additional information. If additional information

 

is requested by an insurer, a prior authorization request under

 

this subsection is considered void if the prescriber fails to

 

submit the additional information within 5 days after the date and

 

time of the original submission of a properly completed standard

 

prior authorization request under this section.

 

     (10) As used in this section:

 

     (a) "Insurer" means any of the following:

 

     (i) An insurer issuing an expense-incurred hospital, medical,

 

or surgical policy or certificate.

 

     (ii) A health maintenance organization.


 

     (iii) A health care corporation operating pursuant to the

 

nonprofit health care corporation reform act, 1980 PA 350, MCL

 

550.1101 to 550.1704.

 

     (iv) A third party administrator of prescription drug benefits.

 

     (b) "Prescriber" means that term as defined in section 17708

 

of the public health code, 1978 PA 368, MCL 333.17708.

 

     (c) "Prescription drug" means that term as defined in section

 

17708 of the public health code, 1978 PA 368, MCL 333.17708.

 

     (d) "Prescription drug benefit" means the right to have a

 

payment made by an insurer pursuant to prescription drug coverage

 

contained within a policy, certificate, or contract delivered,

 

issued for delivery, or renewed in this state.

 

     Enacting section 1. This amendatory act does not take effect

 

unless Senate Bill No. 430 of the 96th Legislature is enacted into

 

law.

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