Estrada, Michele (DIFS)  
From:  
Sent:  
To:  
Miguel Rodriguez <mrodriguez@aprx.org>  
Friday, June 9, 2023 10:09 AM  
Estrada, Michele (DIFS)  
Michael Wright; Ryan Burtka  
Cc:  
Subject:  
Comments of American Pharmacies to Proposed Administrative Rules for Pharmacy  
Benefit Manager Licensure and Regulation Act Rule Set 2023-10 IF  
Comments of American Pharmacies to Rule Set 2023-10 IF 6.9.2023.pdf  
Attachments:  
CAUTION: This is an External email. Please send suspicious emails to abuse@michigan.gov  
Dear Ms. Estrada,  
Attached please find the comments of American Pharmacies to the Proposed Administrative Rules for Pharmacy Benefit  
Manager Licensure and Regulation Act (Rule Set 2023-10 IF)  
Please let me know if you have any questions.  
Thank you,  
Miguel  
Miguel S. Rodriguez  
General Counsel  
1
802 N. Carancahua, Suite 540, Corpus Christi, Texas 78401  
(361) 887-6100  
June 9, 2023  
Via Electronic Mail (EstradaM1@michigan.gov)  
Michele Estrada  
Department of Insurance and Financial Services  
Office of Research, Rules, and Appeals  
P.O. Box 30220  
Lansing, MI 48909-7720  
Re:  
Comments of American Pharmacies to Proposed Administrative Rules for  
Pharmacy Benefit Manager Licensure and Regulation Act  
Rule Set 2023-10 IF  
Dear Ms. Estrada,  
American Pharmacies appreciates the opportunity to present these comments in response  
to the Department of Insurance and Financial Services’ (DIFS) request for comments on the  
administrative rules for the Pharmacy Benefit Manager Licensure and Regulation Act. American  
Pharmacies is a member-owned cooperative. Our members are hundreds of independent pharmacy  
owners located across more than 35 states, including Michigan. Our mission is to protect, defend  
and enhance the business of independent pharmacy so that our members can better serve their  
patients.  
American Pharmacies was a strong supporter of the Pharmacy Benefit Manager Licensure  
and Regulation Act (the “Act”) and our members are looking forward to the full implementation  
of the Act in 2024. The U.S. Supreme Court’s decision in Rutledge v. PCMA, 141 S.Ct. 474 (2020)  
greatly expanded the authority of states to enforce state pharmacy benefit manager (PBM) laws  
like the Act when PBMs are administering claims of ERISA plans. Following Rutledge, courts  
across the country have consistently upheld the power of states to enforce state PBM laws over  
PBMs administering claims for ERISA plans and Medicare Part D plans. See, e.g., PCMA v.  
Wehbi, 18 F.4th 956 (8th Cir. 2021) (holding certain challenged provisions of North Dakota PBM  
reform law were not preempted by ERISA or Medicare Part D); PCMA v. Mulready, 598  
F.Supp.3d 1200 (W.D. Okla. 2022) (holding certain challenged provisions of Oklahoma PBM  
reform law were not preempted by ERISA or Medicare Part D).  
American Pharmacies thanks DIFS for the proposed rules which are an important step  
towards fully implementing the Act and which will rein in many abusive PBM practices while  
increasing the accessibility of Michigan patients to pharmacy services throughout the state. We  
and our members stand ready to work with DIFS to ensure that the Act’s provisions are closely  
adhered to by PBMs in Michigan.  
Page 1 of 2  
We believe that the proposed rules are clearly stated and well supported in the Act.  
Therefore, we are confining our comment to one suggested point of clarification to be included in  
the proposed rules or in subsequent rulemaking.  
Section 11(4) of the Act permits the Director to refuse to issue a license to a PBM that has  
had a PBM “certificate of authority or license denied or revoked for cause in another state.”  
Further, Section 11(5)(e)-(f) of the Act permits the Director to deny, suspend, or revoke the license  
of a PBM if the Director finds that either “any individual responsible for the conduct of affairs of  
the [PBM] has been convicted of, or has entered a plea of guilty or nolo contendere to, a felony  
without regard to whether adjudication was withheld” or that “the [PBM’s] license has been  
suspended or revoked in another state.” Since both of these provisions govern the granting or  
maintenance of a license, we suggest that a new subrule (c)(iv) be added to Rule 500.33 to require  
a PBM to disclose whether these matters have occurred so that the Director is informed and  
remains apprised of any such occurrences.  
American Pharmacies appreciates this opportunity to provide input to DIFS on its  
proposed rules. If I can be of any assistance, please do not hesitate to contact me.  
Yours truly,  
Miguel S. Rodriguez  
General Counsel, American Pharmacies  
Page 2 of 2  
Estrada, Michele (DIFS)  
From:  
Sent:  
To:  
Peter Fjelstad <pfjelstad@pcmanet.org>  
Wednesday, May 31, 2023 5:54 PM  
Estrada, Michele (DIFS)  
Cc:  
Sean Stephenson; Peter Fjelstad  
Subject:  
PCMA Comments on R 500.31 – R 500.39 Pharmacy Benefit Manager Licensure and  
Regulation Act  
Attachments:  
MI DIFS Licensing 5.31.23 (final).pdf  
CAUTION: This is an External email. Please send suspicious emails to abuse@michigan.gov  
Dear Ms. Estrada:  
On behalf of the Pharmaceutical Care Management Association (PCMA), please see the attached comments  
regarding R 500.31 – R 500.39 Pharmacy Benefit Manager Licensure and Regulation Act, as proposed by the  
Michigan Department of Insurance and Financial Services (DIFS).  
We appreciate the opportunity to comment on this proposed rule. And we respectfully request that our attached  
comments be included as part of the record for the DIFS hearing currently scheduled for June 9, 2023.  
If you have any questions, please do not hesitate to contact either myself or my colleague Sean Stephenson,  
CCed on this email.  
Sincerely,  
Peter Fjelstad  
Directory of State Regulatory & Legal Affairs, PCMA  
Peter Fjelstad | PCMA | Director, State Regulatory and Legal Affairs | 202-756-5749  
325 7th Street NW, 9th Floor, Washington, DC 20004  
This is a confidential communication from PCMA that is intended only for the recipients to which it is  
addressed. If you are not the named recipient, or otherwise permitted to review this message on behalf of the  
named recipient, please note that you are not authorized and have no right to review this message. Any  
disclosure, copying, distribution or taking action in relation to the contents of this information is prohibited and  
may be unlawful. Please notify the PCMA sender if you received this message in error and delete all copies.  
1
May 31, 2023  
Michele Estrada  
Department of Insurance and Financial Services, Office of Research, Rules and Appeals  
P.O. Box 30220  
Lansing, MI 48909-7720  
SENT VIA EMAIL  
Re: PCMA Comments on R 500.31 – R 500.39 Pharmacy Benefit Manager Licensure and  
Regulation Act  
Dear Ms. Estrada:  
The Pharmaceutical Care Management Association (“PCMA”) appreciates the opportunity to  
comment on the proposed rules (“Proposed Rule”) published by Michigan’s Department of  
Insurance and Financial Institutions (“DIFS”) on March 14, 2023., This Proposed Rule creates a  
new regulatory framework regarding the licensure of pharmacy benefit managers (“PBMs”) as a  
result of 2022 Public Act 11 (the “Pharmacy Benefit Manager Licensure and Regulation Act”).  
PCMA is the national trade association representing PBMs. PCMA’s member companies  
administer drug benefits for more than 275 million Americans, including most West Virginias,  
who have health insurance through employer-sponsored health plans, commercial health plans,  
union plans, Medicare Part D plans, managed Medicaid plans, the state employee health plan,  
and others.  
Below are PCMA’s comments, concerns, and recommendations regarding specific provisions in  
the Proposed Rule.  
R 500.31 (1)(b) Definitions  
As Drafted: “Client” means any health plan or carrier for which the pharmacy benefit  
manager contracts with a pharmacy or pharmacy services administration organization to  
provide pharmacy health services to covered individuals.  
Proposed Suggested Change:  
Client” means any health plan or carrier for which the pharmacy benefit manager  
contracts with a pharmacy or pharmacy services administration organization to provide  
pharmacy health services to covered individuals. Delete the entire provision as this is  
unsupported by the law.  
1
R 500.33 (2)(b) Application contents and fee; supplemental documents  
As Drafted: A document providing the names, addresses, dates of birth, social security  
numbers, official positions, and professional qualifications of each individual who owns,  
legally or beneficially, 10% or more of the equity in the entity that is applying for a  
license.  
Proposed Suggested Change: A document providing the names, addresses, dates of  
birth, social security numbers, official positions, and professional qualifications of each  
individual officer and director who own, legally or beneficially, 10% or more of the equity  
in the entity that is applying for a license.  
R 500.33 (2)(c)(i) Application contents and fee; supplemental documents  
As Drafted: A list of every client on whose behalf the applicant intends to contract to  
provide pharmacy health services to residents of this state.  
Proposed Suggested Change #1: Delete the provision because it is too burdensome  
for PBMs to list all businesses that it “intends to contract” with.  
Proposed Suggested Change #2: At the time of application, a list of health plans or  
carriers that a PBM contracts with to provide pharmacy health services to individuals  
covered by the health plan or carrier.  
R 500.33 (2)(c)(ii) Application contents and fee; supplemental documents.  
As Drafted: (ii) A list of the staff who shall participate in the applicant’s operations in this  
state. The list must clearly indicate the job functions of each staff member identified.  
Proposed Suggested Change:. (ii) A list of the staff who shall participate in the  
applicant’s operations in this state. The list must clearly indicate the job functions of each  
staff member identified. Delete the entire provision as it is too broad and would be  
difficult for a company to quantify.  
R 500.33 (2)(c)(iii) Application contents and fee; supplemental documents  
As Drafted: A statement indicating all jurisdictions where the applicant has an  
application pending or has been registered, licensed, or otherwise certified to transact  
business as a pharmacy benefit manager.  
Proposed Suggested Change: A statement indicating all jurisdictions where the  
applicant has an application pending or has been registered, licensed, or otherwise  
certified to transact business as a pharmacy benefit manager.  
2
R 500.35(1) Suspension, revocation, and restriction of licensure; fines  
As Drafted: The director may suspend the license of a pharmacy benefit manager as  
provided in sections 11(5) and (6) of the act, MCL 550.821. A pharmacy benefit manager  
whose license is suspended shall not operate within this state as a pharmacy benefit  
manager during the suspension.  
Suggested Changes: Delete the entire provision. If a PBM stops operating in the state,  
then enrollees will not have access to the pharmacy benefits – creating serious patient  
safety issues. An order to revoke a license should not take effect immediately.  
PCMA appreciates the opportunity to comment on the Proposed Rule. We look forward to a  
continued dialogue with DIFS regarding both the Proposed Rule and additional issues as they  
arise. Please feel free to contact either myself or my colleague Sean Stephenson, Director of  
State Affairs (sstephenson@pcmanet.org or 240-909-1544) with any questions or for further  
discussion.  
Sincerely,  
Peter Fjelstad  
Director, State Regulatory & Legal Affairs  
CC: Sean Stephenson  
Director, State Affairs  
3
Estrada, Michele (DIFS)  
From:  
Sent:  
Jill McCormack <JMcCormack@NACDS.org>  
Thursday, June 8, 2023 5:37 PM  
To:  
Estrada, Michele (DIFS)  
NACDS Comments on PBM Licensure and Regulation Act  
MI PBM Licensure Rulemaking Comment Letter06-2023.pdf  
Subject:  
Attachments:  
CAUTION: This is an External email. Please send suspicious emails to abuse@michigan.gov  
Dear Ms. Estrada:  
Thank you for the opportunity to comment on these important proposed rules. Please see our letter attached.  
Thank you,  
Jill  
Jill McCormack | Regional Director, State Government Affairs  
National Association of Chain Drug Stores  
2296 Forest Hills Drive  
Harrisburg, PA 17112  
717.592.8977 (cell)  
1
June 9, 2023ꢀ  
Michele Estrada  
Department of Insurance and Financial Services  
Office of Research, Rules, and Appeals  
P.O. Box 30220, Lansing, MI 48909-7720  
RE: R 500.31 – 500.39 Pharmacy Benefit Manager Licensure and Regulation Act  
Dear Ms. Estrada:ꢀꢀ  
On behalf of our member pharmacies operating in Michigan, the National Association of Chain Drug Stores (NACDS) is  
pleased to submit this letter in support of the Department of Insurance and Financial Services’ (DIFS) proposed rule  
regarding pharmacy benefit manager (PBM) licensure and regulation. We urge the Department to bring to bear its full  
enforcement authority to ensure that PBMs operating in the state do not bypass laws meant to support pharmacies as  
they fulfill their duty to deliver reliable services to the patients who trust them.  
NACDS supported the Michigan Legislature’s efforts in 2022 to pass comprehensive legislation that would provide relief  
to the state’s pharmacies and patients from the unfair and abusive tactics commonly employed by PBMs. The proposed  
rules would add another layer of protection by giving the Department enforcement authority to uncover and penalize  
PBM misconduct, including revoking the ability of PBMs to operate in the state if they do not comply.  
Another crucial piece in enforcement is the ability for DIFS to uncover wrongful conduct based on complaints filed by  
patients and pharmacies. A public complaint process will help provide DIFS with a line of sight into PBM tactics  
prohibited by the Act that directly affect patients and pharmacies at the store level. Therefore, NACDS asks that the  
Department develop a simple and reliable filing process for complaints.  
Additionally, NACDS wishes to affirm its understanding that the state has the authority to establish statutory minimum  
and other standards for PBMs that serve state-regulated health plans. And to a limited extent, states may also regulate  
PBMs that serve self-insured Employee Retirement Income Security Act of 1974 (ERISA)-regulated group health plans.  
Under PCMA v. Rutledge, the U.S. Supreme Court determined that state regulations that do not directly affect “central  
matters of plan administration or interfere with nationally uniform plan administration” are not preempted by ERISA.  
Accordingly, we encourage the state to ensure the application of the protections of the law to self-insured plans, in the  
same way, it would for other plans, to the extent the law does not directly impact plan administration.  
NACDS thanks DIFS for the opportunity to comment on this proposed rule and applauds the Department for taking this  
key step in the process to ensure PBM accountability and transparency.ꢀFor questions or further discussion, please  
contact Jill McCormack, Director of State Government Affairs, at JMcCormack@nacds.org.  
Sincerely,  
Steven C. Anderson, FASAE, CAE, IOM  
President and Chief Executive Officer  
1776 Wilson Blvd., Suite 200, Arlington, VA 22209  
P: 703.549.3001  
F: 703.836.4869  
NACDS.org  
Estrada, Michele (DIFS)  
From:  
Sent:  
Anne Cassity <anne.cassity@ncpa.org>  
Tuesday, May 2, 2023 4:58 PM  
To:  
Estrada, Michele (DIFS)  
NCPA Comments on Rules Implementing Act No. 11, Public Acts of 2022 (H.B. 4348)  
Final_NCPA comments on rules implementing Act No 11, Public Acts 2022_HB 4348.pdf  
Subject:  
Attachments:  
CAUTION: This is an External email. Please send suspicious emails to abuse@michigan.gov  
Dear Ms. Estrada,  
On behalf of the Naꢀonal Community Pharmacists Associaꢀon (NCPA), I am submiꢁng comments on rules implemenꢀng  
Act. No. 11, Public Acts of 2022, which encourages the Department to fully implement House Bill 4348.  
NCPA represents the interests of the owners, managers, and employees of more than 19,000 independent community  
pharmacies across the United States, including 801 independent community pharmacies in Michigan. These Michigan-  
based pharmacies employ more than 9,800 residents and filled nearly 51 million prescripꢀons in 2021 alone.  
Thank you for your aꢂenꢀon and consideraꢀon.  
Anne Cassity  
SVP, Government Affairs  
National Community Pharmacists Association  
100 Daingerfield Road  
Alexandria, Virginia 22314-2888  
703.838.2682 direct  
703.282.9906 mobile  
1
VIA ELECTRONIC MAIL  
May 2, 2023  
Michele Estrada  
Michigan Department of Insurance and Financial Services  
Office of Research, Rules, and Appeals  
530 West Allegan Street, 7th Floor  
Lansing, MI 48933  
Re:  
Dear Ms. Estrada:  
As you know, on February 23, 2022, Governor Gretchen Whitmer signed House  
Comments on Rules Implementing Act No. 11, Public Acts of 2022 (H.B. 4348)  
Bill 4348 into law. Now known as Public Act 11 of the Public Acts of 2022, the law  
regulates the anticompetitive practices of pharmacy benefit managers or PBMs.  
House Bill 4348 was a crowning achievement for Governor Whitmer, whose  
Prescription Drug Task Force had recommended its enactment into law. As she noted  
upon signing the legislation, “For too long, unlicensed pharmacy benefit managers have  
been able to engage in practices that drive up costs for Michiganders whose lives and  
health depend on critical prescription drugs like insulin.” It is therefore no wonder House  
Bill 4348 achieved final passage in the House 101 to 4 and in the Senate 30 to 9.  
In light of the legislation’s overwhelming bipartisan support, we were a bit  
surprised—and frankly disappointed—to see that your Department has failed to propose  
regulations needed to fully implement the legislation. House Bill 4348 includes  
comprehensive provisions designed to regulate the anti-competitive business practices  
of PBMs. But rather than address this conduct, your Department has proposed only to  
clarify the rules around the process for applying for, renewing, and suspending a PBM’s  
license. See Proposed Rules on Pharmacy Benefit Manager Licensure and Regulation  
(Mar. 13, 2023). Put simply, more is needed to help Governor Whitmer and the  
Legislature achieve their vision of holding PBMs accountable.  
As the voice for independent pharmacy, the National Community Pharmacists  
Association (NCPA) submits these comments to encourage you to complete the  
Department’s important work—by fully implementing House Bill 4348. Founded in 1898,  
NCPA represents the interests of the owners, managers, and employees of more than  
19,000 independent community pharmacies across the United States, including 801  
independent community pharmacies in Michigan. These Michigan-based pharmacies  
employ more than 9,800 residents and filled nearly 51 million prescriptions in 2021 alone.  
And overall, NCPA’s members employ over 239,000 individuals on a full or part-time  
basis and dispense roughly 40% of the nation’s retail prescriptions.  
We have organized our comments into two main sections. First, we explain the  
reasons why the State of Michigan enacted House Bill 4348, including the anticompetitive  
practices of PBMs giving rise to the legislation. Second, we explain places where the  
Department should promulgate regulations to implement the legislation consistent with  
the text and purpose of the law.  
NCPA is committed to offering our assistance as the Department works through  
the rulemaking process.  
I.  
The Reasons Michigan Enacted House Bill 4348  
House Bill 4348 was enacted against an evolving backdrop: PBMs have assumed  
an outsized role in limiting access to prescription drugs while increasing costs for  
patients, and the Supreme Court of the United States recently clarified the important part  
States play in regulating PBMs.  
A.  
Abusive PBM Business Practices  
Pharmacy benefit managers are not health plans or insurers. Rather, “PBMs serve  
as intermediaries between prescription-drug plans and the pharmacies that beneficiaries  
use.” Rutledge v. Pharm. Care Mgmt. Ass’n, 141 S. Ct. 474, 478 (2020). PBMs enter into  
contracts with benefit plans and insurers to provide beneficiaries with access to  
prescription drugs. PBMs deliver this access by contracting separately with pharmacies  
to create networks where beneficiaries can fill their prescriptions. Notably, the three  
largest PBMs claim to provide benefit-management services for more than 268 million  
Americans—which amounts to over eighty-five percent of all Americans with health  
insurance.  
As a third-party service provider, PBMs are under no obligation to act in the best  
interests of the plans and patients they purport to serve—and frequently they do not. For  
example, PBMs derive a significant portion of their revenue by charging plans one price  
for prescriptions and then reimbursing pharmacies at a lesser amount—keeping the  
difference as profit. PBMs consider their price lists proprietary and do not disclose them  
to the plans they claim to serve. For instance, when the State of Ohio investigated the  
PBMs responsible for servicing the State’s Medicaid plans, it discovered that PBMs had  
realized undisclosed profits of $224.8 million off this difference in a single year—all to  
2
the detriment of taxpayers. Dave Yost, Ohio’s Medicaid Managed Care Pharmacy Services  
1
Auditor of State Report 2 (Aug. 16, 2018).  
Separately, PBMs have had a negative effect on pharmacy. Because the three  
largest PBMs dominate the market, pharmacies have limited bargaining power when  
negotiating with PBMs. Refusing to accept a PBM’s contract could mean the inability to  
serve the majority of patients in a pharmacy’s community. As a result, PBM-pharmacy  
contracts generally grant PBMs unilateral authority to dictate the amount of  
reimbursement paid to pharmacies for generic drugs, require pharmacies to fill and  
dispense prescriptions regardless of the amount the pharmacy is reimbursed, and impose  
a variety of other restrictions on the practice of pharmacy. For example, PBMs have  
barred pharmacists from informing patients of instances in which the patient could pay  
less out of pocket for a prescription drug than that patient would pay if the claim were  
processed through the PBM.  
Evidence suggests that PBM reimbursement practices have driven more than  
sixteen percent of independent rural pharmacies out of business. Abiodun Salako et al.,  
Update: Independently Owned Pharmacy Closures in Rural America, 2003-2018, RUPRI Center  
2
for Rural Health Policy Analysis (July 2018). This, in turn, means that Americans—  
particularly in underserved areas—can face barriers to accessing lifesaving medications.  
PBMs also own mail-order pharmacies that compete directly with the retail  
pharmacies in a PBM’s network, and PBMs have used their position as middleman to  
steer—and even force—patients to use PBM-affiliated pharmacies. This practice  
negatively affects patients in at least three ways. First, it requires patients to go through  
mail-order pharmacies for medications that are otherwise available at their corner drug  
store. Second, some PBM-affiliated pharmacies have experienced delays in timely filling  
orders and have spoiled temperature-sensitive medication. Alex Smith, Extreme  
3
Temperatures May Pose Risks To Some Mail-Order Meds, NPR, Jan. 7, 2019. Finally, many  
PBMs engage in the highly questionable practice of reimbursing their own affiliated  
pharmacies substantially more than they pay non-affiliated pharmacies. CVS Caremark,  
for example, paid CVS pharmacies forty-six percent more for generic drugs than it paid  
pharmacies at Walmart and Sam’s Club. Marty Schladen & Cathy Candisky, CVS paid  
itself far more than some major competitors, Columbus Dispatch, Jan. 20, 2019 (citing a report  
4
by the State of Ohio). And CVS Caremark paid itself over five times as much as it  
reimbursed independent pharmacies in Arkansas for some medications—or $324.91  
1 https://ohioauditor.gov/auditsearch/Reports/2018/Medicaid_Pharmacy_Services_2018_Franklin.pdf.  
2 https://rupri.public-health.uiowa.edu/publications/policybriefs/2018/  
2018%20Pharmacy%20Closures.pdf.  
3 https://www.npr.org/sections/health-shots/2019/01/07/673806506/extreme-temperatures-may-pose-  
risks-to-some-mail-ordermeds.  
4 https://www.dispatch.com/news/20190120/cvs-paid-itselffar-more-than-some-major-competitors-  
report-says.  
3
more on a single transaction. Linette Lopez, What CVS is doing to mom-and-pop pharmacies  
5
in the US will make your blood boil, Business Insider, Mar. 30, 2018. As a result, there is  
substantial evidence that PBM steering—an inherent conflict of interest—not only  
decreases access to medications, but also increases costs to plans and their patients.  
B.  
House Bill 4348  
In response to these and other practices, Michigan enacted House Bill 4348, which  
mirrors a wave of legislative activity across the country. Indeed, nearly every State—big  
and small; red and blue—has enacted laws regulating PBMs. In addition, the Attorneys  
General of forty-six States (Michigan included) and the District of Columbia signed onto  
briefs in the Supreme Court of the United States making clear that States have robust  
authority to regulate in this space—a position that the Supreme Court affirmed  
unanimously in Rutledge.  
House Bill 4348 includes a number of key features borrowed from the successes of  
sister States, including Arkansas and North Dakota. Notably, PBMs had attempted to  
challenge many of these provisions in court, but they have been rebuffed by the Supreme  
Court and other federal courts. As a result, most of the provisions of House Bill 4348 have  
already withstood legal challenge—and all are safely defensible.  
1.  
Section 11 – Licensing  
The first substantive section of House Bill 4348, Section 11, requires PBMs to obtain  
a license to offer their services in the State of Michigan. It defines the basic obligations for  
a PBM to apply for a license, sets forth a process for renewal, and authorizes the Director  
of the Department of Insurance and Financial Services to suspend or revoke a PBM’s  
license in certain circumstances.  
3.  
Section 13 – Director’s Authority to Promulgate Regulations  
Section 13 provides that the Director “shall” promulgate “rules that are necessary  
or required to implement this act.” In addition, Section 13 provides that, in exercising her  
authority, the Director “must” promulgate rules that “include fines, suspension of  
licensure, restriction of licensure, and revocation of licensure in according with this act.”  
3.  
Section 15 – Duty of Good Faith and Fair Dealing  
Section 15 provides that a PBM shall exercise “good faith and fair dealing” in the  
performance of its contractual duties to both health plans and network pharmacies.  
Notably, the phrase “good faith and fair dealing” is undefined.  
The remaining subsections of Section 15 spell out several specific duties that PBMs  
owe. Among other things, PBMs:  
5 https://www.businessinsider.com/cvs-squeezing-us-momand-pop-pharmacies-out-of-business-2018-3.  
4
must notify the health plans they serve in writing of potential conflicts of  
interest;  
may not charge a pharmacy a fee related to a claim or reduce the amount of  
the claim at the time of the claim’s adjudication or after the claim is  
adjudicated; and  
except for the recoupment of money following an audit done in  
conformance with the law, a PBM may not recoup money from a pharmacy  
that has been paid unless authorized by law.  
4.  
Section 17 – Regulation of PBM-Pharmacy Networks  
Section 17 of House Bill 4348 regulates the quality of the networks that PBMs sell  
to health plans in the State of Michigan. As noted above, PBMs create networks by  
contracting with pharmacies and then sell plans access to these networks.  
Subsection 1 of Section 17 states that a PBM shall provide a “reasonably adequate  
and accessible retail pharmacy benefit manager network for the provision of drugs for a  
health plan that must provide for convenient enrollee access to pharmacies within a  
reasonable distance from an enrollee’s residence, as determined by the director.”  
Notably, the phrases “reasonably adequate and accessible” and “reasonable distance” are  
not defined.  
Subsections 2 through 5 require PBMs to file reports on network adequacy and  
allow the director to grant a waiver from the law’s adequacy requirements if the PBM  
satisfies certain conditions.  
The remaining subsections focus on a PBM’s relationship with its network  
pharmacies. Subsection 6 bans PBMs from conducting spread pricing in Michigan, and  
subsection 7 precludes PBMs from charging pharmacies a fee to process claims.  
5.  
Section 19 – Regulation of PBM Business Practices  
Section 19 regulates anti-competitive business practices of PBMs, including  
discrimination against nonaffiliated pharmacies and favoritism of pharmacies in which  
the PBM has an ownership interest. This includes provisions aimed at forcing and  
steering patients to affiliated PBM pharmacies and penalizing or discouraging patients  
for using unaffiliated pharmacies.  
6.  
Section 21 – Patient Access to Fair Information and Pricing  
Section 21 ensures that patients have access to fair information about the drugs  
they have been prescribed, including information about the cost of those drugs and more  
affordable alternatives. This provision effectively bans PBMs from imposing gag clauses  
that had restricted pharmacies from providing this information to their patients. In  
5
addition, Section 21 prohibits a PBM from charging a copayment or cost-sharing amount  
to a patient that exceeds the cost of the patient’s medication.  
7.  
Section 23 – PBM Transparency Reporting  
Section 23 requires PBMs to file transparency reports with the Director. These  
reports require the disclosure of aggregate information about costs, rebates, fees, and  
reimbursement amounts, among other things. The section specifically precludes the  
disclosure of any information that would identify a specific health plan or enrollee, or the  
specific price charged for a specific drug.  
8.  
Section 27 – Regulation of PBM Maximum Allowable Cost Lists  
Section 27 regulates the use of maximum allowable cost (MAC) lists, which are the  
principal means by which PBMs reimburse pharmacies for dispensing generic drugs.  
Notably, PBMs keep their pricing lists secret, maintain more than one MAC list, and  
sometimes reimburse pharmacies under these lists less than any pharmacy could acquire  
the drug in question. Under Section 27, PBMs must provide pharmacies with access to  
their MAC lists, update those lists at least once every 7 days; and provide pharmacies  
with a reasonable appeals process for challenging a reimbursement under a MAC list.  
9.  
Section 28 – Fair Audits  
Section 28 places limitations on a PBM’s ability to audit a pharmacy. Among other  
things, this section requires PBMs to provide advanced written notice of an audit, places  
limitations on the substance of such an audit (such as by requiring a PBM to employ a  
pharmacist if the audit turns on clinical judgments), and sets up an appeals process.  
10.  
Section 29 – Regulation of PBM Restrictions on Pharmacy  
Section 29 places limitations on a PBM’s ability to place restrictions on the services  
that pharmacies can perform. For example, Section 29 provides that a pharmacy may  
deliver certain drugs to a patient, limits a PBM’s ability to impose accreditation or  
recertification standards in excess of State licensing standards, and prohibits PBMs from  
retaliating against pharmacists for availing themselves of the protections of the Act.  
11.  
Section 30 – Enforcement of the Act by the Director  
Section 30 provides that the Director shall enforce the Act. It also empowers the  
Director to examine or audit the books and records of PBMs.  
12.  
Section 31 – PBM Compliance with the Act  
Section 31 provides that a contract between a PBM and an insurer that exists on  
the date of licensure of the PBM must comply with the requirements of the Act as a  
condition of the PBM’s license.  
6
13.  
Section 33 – Retention of Records  
Section 33 provides that the Director shall establish a retention schedule for all  
records, books, papers, and other data on file with the Department related to the  
enforcement of the Act.  
14.  
Section 35 – Clarification on Interaction with Federal Law  
Section 35 provides that the Act shall be applied on a claim-by-claim basis, and  
that the Act does not apply only “with respect to a claim that is entirely preempted by  
federal law, including Medicare Part D or the employee retirement income security act”  
(also known as ERISA).  
15.  
Effective Date  
The Act takes effect January 1, 2024.  
II.  
Provisions the Department Should Implement Through Regulations  
In the section that follows, we discuss those portions of the new law where,  
consistent with Section 13, regulations are “necessary or required” to implement the Act.  
In particular, the Department should promulgate regulations that address six major areas  
of the new law: (A) clarifying the limited scope of the provision on federal preemption,  
(B) defining the “duty of good faith and fair dealing,” (C) establishing standards for  
determining whether a PBM’s network is “reasonably adequate and accessible,” and  
includes pharmacies within a “reasonable distance” of an enrollee; (D) clarifying the  
scope of a PBM’s duties not to discriminate against “nonaffiliated” pharmacies;  
(E) defining Maximum Allowable Cost (MAC) lists to ensure PBMs cannot engage in  
semantics to evade compliance with the law; and (F) establishing the steps the Director  
will take to enforce the law.  
A.  
Regulations Clarifying the Limited Scope of the Provision on Preemption  
As noted above, Section 35 provides that the “act does not apply with respect to a  
claim that is entirely preempted by federal law,” including ERISA and Medicare Part D.  
Although it may appear obvious, the Director should clarify that the Act applies  
to claims that are not entirely preempted by federal law, including claims not entirely  
preempted by ERISA and Medicare Part D. As it stands now, opponents of the Act could  
argue that it does not apply whenever a PBM is handling a claim involving a plan  
regulated by ERISA or Medicare Part D. That would not be a fair or accurate  
interpretation of the language of Section 35. But because Section 35 clarifies the scope of  
the new law, it is imperative that the Director speak clearly on when she has authority to  
enforce the new law.  
In interpreting Section 35, the Director’s task is to give meaning to the words  
selected by the Legislature. Here, the Legislature rejected any interpretation of the Act  
7
that would prevent it from applying wholesale to PBMs serving plans regulated by  
ERISA and Medicare Part D.  
For one thing, the Legislature did not say that the Act could not apply to PBMs  
serving plans regulated by ERISA and Medicare Part D. Quite the opposite, the  
Legislature said that the Act does not apply only with respect to a “claim” that is  
“entirely” preempted by federal law.  
By using the term “claim,” Section 35 clarifies that any preemption analysis must  
be conducted on a claim-by-claim basis. That’s because “claim” is a defined term that  
“means a request for payment for administering, filling, or refilling a drug or for  
providing a pharmacy service or medical supply or device to an enrollee.” H.B. 4348  
§ 5(d).  
Similarly, by using the term “entirely,” the Legislature clarified that the Act would  
apply to a claim to the extent it is not completely preempted by ERISA or Medicare Part  
D. After all, the plain meaning of the term “entirely” means “completely.”  
In addition, this understanding of Section 35 is consistent with the legal backdrop  
under which House Bill 4348 was passed. As noted above, shortly before the Legislature  
enacted House Bull 4348, the Supreme Court of the United States clarified that ERISA  
does not completely preempt State laws that apply to PBMs—even when PBMs are  
providing services to plans that are subject to regulation by ERISA. And federal courts  
have expressed similar views about Medicare Part D. In PCMA v. Wehbi, for example, the  
U.S. Court of Appeals for the Eighth Circuit explained that Medicare Part D “does not  
preempt all state laws as applied to Medicare Part D; rather, it preempts only those that  
occupy the same ‘place’—that is, that regulate the same subject matter as—federal  
Medicare Part D standards.” 18 F.4th 956, 971 (8th Cir. 2021).  
Together, this strongly suggests that the Legislature wanted to limit the scope of  
the Act to only those “claims” that are “entirely” preempted by federal law. Otherwise,  
to the extent that an individual claim is not preempted by federal law, the State of  
Michigan can—and should—enforce its law. The Director’s clarification around this issue  
is therefore critical.  
B.  
Regulations Clarifying the “Duty of Good Faith and Fair Dealing”  
Section 15 provides that a PBM shall exercise “good faith and fair dealing” in the  
performance of its contractual duties to both health plans and network pharmacies.  
Critically, however, the phrase “good faith and fair dealing” is undefined.  
The Director should promulgate regulations defining the statutory duty of good  
faith and fair dealing imposed by Section 15. And the Director should clarify that this  
statutory duty is distinct from the contractual duty of good faith and fair dealing that is  
presumed to exist in the performance of all contracts under Michigan law (except  
8
employment contracts). See Hammond v. United of Oakland, Inc., 193 Mich. App 146, 151–  
152 (1992).  
Opponents of the legislation may argue that the statutory duty is indistinct from  
the contractual duty that exists in all contracts, but they would be wrong. For one thing,  
if the opponents were correct, then there would have been no need for the Legislature to  
have created a statutory duty of good faith and fair dealing, because, as noted just above,  
courts already impose a contractual duty of good faith and fair dealing. In divining the  
will of the Legislature, the Director should avoid any interpretation of the Act that would  
render any of its provisions superfluous. E.g., Danto v. Michigan Bd. of Med., 168 Mich.  
App. 438, 442 (1988). And that means that the statutory duty of good faith and fair dealing  
must mean something different than the general duty of good faith and fair dealing that  
arises by contract.  
As for substance, the Director should clarify that the statutory duty of good faith  
and fair dealing requires that:  
a PBM may not reimburse a pharmacy less than the pharmacy’s cost to  
acquire a drug, because such action is inconsistent with, and would  
frustrate, the common understanding of “reimburse,” which means to  
“repay”;  
a PBM must pay a reasonable dispensing fee, separate and apart from  
whatever the PBM reimburses a pharmacy for a drug, to ensure that the  
PBM has reimbursed the pharmacy for the full cost of its services, which  
includes both the acquisition cost of its drug and overhead on any given  
prescription;  
a PBM may not accept a rebate or other payment from a pharmaceutical  
manufacturer that is not completely and fully disclosed to the health plan  
or third-party payor that the PBM purports to serve; and  
a PBM must disclose to the health plan or third-party payor that the PBM  
purports to serve the difference between what the PBM charges the health  
plan or third-party payor and what it reimburses pharmacies in the  
aggregate for the drugs it processes for the health plan or third-party payor;  
These provisions are all necessary to give meaning to the statutory duty of good faith and  
fair dealing that the Legislature has imposed upon PBMs in their relationships with  
pharmacies and health plans. As noted above, in the absence of these specific duties,  
PBMs have engaged in abusive behavior that has frustrated the reasonable expectations  
of the pharmacies and plans that contract with PBMs.  
In addition, in Rutledge, the Supreme Court of the United States held that ERISA  
does not preempt State laws that regulate the economic relationship among PBMs,  
9
pharmacies, and ERISA plans. See 141 S. Ct. at 480-81. Thus, there is no legal obstacle to  
promulgating regulations of the type outlined above.  
C.  
Regulations Defining the Standards for PBM-Pharmacy Networks  
Section 17 of House Bill 4348 regulates the quality of the networks that PBMs sell  
to health plans in the State of Michigan. As noted above, the section imposes a duty on  
PBMs to ensure that their pharmacy networks are “reasonably adequate and accessible”  
and a “reasonable distance” to enrollees. But not one of these quoted terms is defined.  
The Director should promulgate regulations that define a PBM’s duties to create  
adequate and accessible pharmacy networks within the State of Michigan. Although less  
than perfect, as a stopgap, the Director should adopted the network adequacy standards  
established by the Centers for Medicare and Medicaid Services (CMS) that apply to plans  
subject to regulation under Medicare Part D. See 42 C.F.R. § 423.120. But the Director  
should make one important tweak to these stopgap standards: Unlike CMS’s access  
standards, the Director’s standards should apply to both standard and preferred  
networks.  
Once the Director implement’s CMS’s network adequacy standards as a stopgap  
that apply to both standard and preferred networks in the State of Michigan, the Director  
should solicit comments on changes to Michigan’s network adequacy standards to ensure  
that they provide sufficient access to retail pharmacies throughout the State—including  
the State’s rural and urban markets.  
In the absence of clear guidance upfront as to what is expected of PBMs, it will be  
next to impossible for the Director to ensure compliance on a case-by-case basis with the  
Legislature’s otherwise undefined network adequacy standards. In addition, without  
clear guidance, PBMs and pharmacies will not know the rules by which PBMs are being  
judged.  
D.  
Regulations Defining a PBM’s Duty Not to Discriminate  
Among Section 19’s prohibitions, it provides that a PBM “shall not discriminate  
against a nonaffiliated pharmacy that is a retail pharmacy.” The Act does not define the  
scope of this prohibition.  
The Director should clarify that a PBM’s duty includes not discriminating against  
a nonaffiliated retail pharmacy that wishes to join a PBM’s standard or preferred  
pharmacy network, provided that pharmacy is willing and able to abide by the terms and  
conditions for network participation. In the absence of such a prohibition, PBMs have  
regularly discriminated against retail pharmacies in an effort to steer patients to PBM-  
affiliated mail-order pharmacies. This is not only anti-competitive, but also limits patient  
access to prescription medications at their corner drugstores.  
10  
Increasingly, States are enacting such anti-discrimination measures, which are also  
known as any-willing-provider (AWP) provisions. A federal district court in Oklahoma  
recently blessed such a provision, see PCMA v. Mulready, 598 F. Supp. 3d 1200, 1207-08  
(W.D. Okla. 2022); the Attorney General of Michigan signed onto an amicus curiae brief  
expressing the view that ERISA does not preempt such a provision, see Br. of 34 States  
and the District of Columbia as Amici Curiae, No. 22-6074 (10th Cir. filed Oct. 18, 2022);  
and the United States government filed a brief taking a similar position that State AWP  
provisions are not preempted by ERISA as applied directly to third-party PBMs, see Br.  
of United States as Amicus Curiae, PCMA v. Mulready, No. 22-6074 (10th Cir. filed Apr. 10,  
2023). Thus, there is explicit authority for promulgating such a requirement.  
In addition, the Director should promulgate regulations providing that PBMs may  
not reimburse an affiliated pharmacy more than an unaffiliated pharmacy that operates  
in the same network as the affiliated pharmacy—whether standard or preferred.  
Otherwise, PBMs have engaged in discriminatory reimbursement practices that have  
forced the closure of independent pharmacies. As noted above, CVS Caremark has  
reimbursed CVS pharmacies five times more than independent pharmacies. Linette Lopez,  
What CVS is doing to mom-and-pop pharmacies in the US will make your blood boil, Business  
Insider, Mar. 30, 2018. Adding insult to injury, after under-reimbursing independent  
pharmacies CVS sent letters to pharmacists in Arkansas and Ohio stating that selling their  
businesses to CVS was an “attractive and practical option” in the face of “declining  
reimbursements.” Id. (linking to CVS letter).  
Finally, the Director should promulgate regulations providing that PBMs may not  
charge enrollees different copayment or cost sharing amounts at un-affiliated pharmacies  
than the PBM charges at affiliated pharmacies within the same network—whether  
standard or preferred. PBMs have otherwise used the discriminatory practices to steer  
patients to their own pharmacies—which often charge higher fees to the health plans the  
PBMs purport to serve.  
E.  
Regulations Further Defining Maximum Allowable Cost  
Section 27 regulates how PBMs may use maximum allowable cost (MAC) lists to  
reimburse pharmacies for generic drugs. Section 7(c) defines maximum allowable cost to  
mean “the maximum amount that a pharmacy benefit manager will reimburse a network  
pharmacy for the ingredient cost for a generic drug.” Together, the purpose behind these  
provisions is to ensure that PBMs employ a fair process for reimbursing pharmacies for  
generic drugs.  
Unfortunately, when faced with similar provisions in other jurisdictions, PBMs  
have engaged in a game of semantics, calling their MAC lists something else, and then  
claiming that a given State’s laws no longer applied. For that reason, States like Arkansas  
have been forced to re-define the term MAC to ensure that PBMs cannot evade the  
purpose of MAC-based legislation, which is to ensure a fair process for reimbursing  
pharmacies for dispending generic drugs. See Ark. Code § 17-92-507(a)(1)(A) & (B).  
11  
As a result, the Director should promulgate regulations that define MAC broadly  
to include any label attached by a PBM defining the process for reimbursing pharmacists  
for generic drugs. Taken the lead for Arkansas, the Director’s regulation should provide:  
“Maximum Allowable Cost List” means a listing of drugs or other  
methodology used by a pharmacy benefits manager, directly or indirectly,  
setting the maximum allowable cost on which reimbursement payment to  
a pharmacy or pharmacist may be based for a generic drug, brand-name  
drug, biologic product, or other prescription drug.  
“Maximum Allowable Cost List” includes without limitation:  
(i) Average acquisition cost, including national average drug  
acquisition cost;  
(ii) Average manufacturer price;  
(iii) Average wholesale price;  
(iv) Brand effective rate or generic effective rate;  
(v) Discount indexing;  
(vi) Federal upper limits;  
(vii) Wholesale acquisition cost; and  
(viii) Any other term that a pharmacy benefits manager or a healthcare  
insurer may use to establish reimbursement rates to a pharmacist  
or pharmacy for pharmacist services.  
F.  
Regulations Ensuring PBM Compliance with House Bill 4348  
Finally, House Bill 4348 imposes various duties that PBMs owe to pharmacies. As  
examples, Section 27 regulates the use by PBMs of MAC lists, and Section 28 places  
limitations on a PBM’s ability to audit a pharmacy. Notably, these provisions are silent  
on enforcement.  
The Director should promulgate regulations that allow pharmacies to petition the  
Department to bring an enforcement action against a PBM for non-compliance with the  
House Bill 4348. Such a regulation would be consistent with Section 30, which provides  
that the Director “shall enforce this act.” Indeed, by soliciting petitions from pharmacies  
and developing an orderly system for adjudicating their claims, the Director would tap  
into a wealth of information about alleged PBM non-compliance.  
The enforcement protocols established by the Director should include: (1) a  
standardized form that allows a pharmacy, pharmacist, or pharmacy services  
administrative organization to quickly and easily file an administrative complaint with  
12  
the Department; (2) an electronic system for submitting such complaints and tracking the  
Department’s investigation and resolution of any such complaint; (3) allowance for the  
Director to delegate her adjudicative function to subordinate employees of the  
Department and hold fact-finding hearings to adjudicate complaints; and  
(4) establishment of a process for timely resolution of such complaints.  
* * * * *  
As we explained at the outset, House Bill 4348 is intended to regulate anti-  
competitive practices by PBMs that have increased costs while limiting patient choice. It  
is modeled off legislation adopted by other States, and its provisions have already  
survived legal challenges mounted by PBMs. As such, there are no valid legal obstacles  
to promulgating the regulations proposed in these comments.  
NCPA is committed to helping the Department of Insurance and Financial  
Services to ensure that the laudable goals of this legislation are fully realized.  
Very truly yours,  
Anne Cassity  
Senior Vice President of Government Affairs  
National Community Pharmacists Association  
13  
Estrada, Michele (DIFS)  
From:  
Sent:  
Eric Roath <eroath@michiganpharmacists.org>  
Friday, June 9, 2023 2:31 PM  
To:  
Cc:  
Estrada, Michele (DIFS)  
Mark Glasper; Farah Jalloul; Sammy Salem  
Michigan Pharmacists Association Comments on PBM Rules  
Pharmacy PBM Comments 06-2023.pdf  
Subject:  
Attachments:  
CAUTION: This is an External email. Please send suspicious emails to abuse@michigan.gov  
Michele Estrada,  
Please consider the aꢀached comments related to the proposed rules for Pharmacy Benefit Manager Licensure and  
Regulation. Please reach out to me if you have any questions regarding our comments. We would be delighted to be a  
resource for you and your team.  
Sincerest thanks,  
Eric Roath, PharmD, MBA  
Director of Government Affairs  
Michigan Pharmacists Association  
408 Kalamazoo Plaza, Lansing, MI 48933  
Cell (906) 282-8930  
Direct (517) 377-0254  
1
Michele Estrada  
Department of Insurance and Financial Services,  
Office of Research, Rules, and Appeals,  
P.O. Box 30220  
Lansing, MI 48909-7720  
Thank you for the opportunity to provide comments on the Rules for Pharmacy Benefit Manager Licensure  
and Regula�on. Michigan Pharmacists Associa�on (MPA) represents pharmacy prac��oners across the  
state of Michigan. We represent pharmacists and pharmacy technicians in all prac�ce areas, from  
community outpa�ent prac�ce to inpa�ent health systems.  
The proposed rules regarding licensure are an excellent start. S�ll, we feel that there are certain  
ambigui�es in the statute that merit further clarifica�on. We humbly request that addi�onal rules be  
promulgated to address the following concerns:  
Good Faith and Fair Dealing  
I.  
GOOD FAITH AND FAIR DEALING  
Public Act 11, 2022  
Sec. 15. (1) A pharmacy benefit manager shall exercise good faith and fair dealing in the performance of  
its contractual duꢀes to a health plan or network pharmacy. A provision in a contract that aꢁempts to  
waive or limit the obligaꢀon under this subsecꢀon is void.  
MPA recognizes that the phrase “good faith and fair dealing” have not been adequately defined. We  
request an addi�on to the promulgated rules that defines this term to meet the following condi�ons:  
A pharmacy benefit manager shall exercise good faith and fair dealing in the performance of its  
contractual du�es. Therefore:  
1. A PBM may not reimburse a pharmacy less than the pharmacy’s cost to acquire a drug, because  
such ac�on is inconsistent with, and would frustrate, the common understanding of  
“reimburse,” which means to “repay.”  
2. A PBM must pay a reasonable dispensing fee, separate and apart from whatever the PBM  
reimburses a pharmacy for a drug, to ensure that the PBM has reimbursed the pharmacy for the  
full cost of its services, which includes both the acquisi�on cost of its drug and overhead on any  
given prescrip�on. Minimum dispensing fees shall be:  
a. The professional dispensing fee for drugs indicated as specialty medica�ons is $15 or  
the pharmacy’s submited dispensing fee, whichever is less.  
b. The professional dispensing fee for all other drugs is $8.10 or the pharmacy’s submited  
dispensing fee, whichever is less.  
3. A PBM may not accept a rebate or other payment from a pharmaceu�cal manufacturer that is  
not completely and fully disclosed to the health plan or third-party payor that the PBM purports  
to serve; an  
4. A PBM must disclose to the health plan or third-party payor that the PBM purports to serve the  
difference between what the PBM charges the health plan or third-party payor and what it  
reimburses pharmacies in the aggregate for the drugs it processes for the health plan or third-  
party payor.  
MPA recognizes that dispensing fees vary across the state. In accordance with CMS regula�ons, the State  
of Michigan has conducted a cost of dispensing study and determined es�mates for the cost of dispensing  
for different classes of medica�ons. We have suggested that a “reasonable” cost of dispensing by placed  
at 75% of what has been determined by the study conducted by the State of Michigan.  
II.  
Reasonable and Adequate Access:  
Public Act 11, 2022  
Sec. 17. (1) A pharmacy benefit manager shall provide a reasonably adequate and accessible retail  
pharmacy benefit manager network for the provision of drugs for a health plan that must provide for  
convenient enrollee access to pharmacies within a reasonable distance from an enrollee’s residence, as  
determined by the director.  
MPA recognizes that the phrase, “reasonably adequate and accessible” and “reasonable distance” is not  
defined. We reques�on an addi�on to the promulgate rules that defines this as:  
Reasonably and adequate and accessible,” means having a pharmacy within a reasonable  
distance of the pa�ent’s home address.  
“Reasonable distance,” means a distance consistent with 42 CFR § 423.120.  
III.  
Non-discriminaꢀon against nonaffiliated pharmacies  
Public Act 11, 2022  
Sec. 19. (1) A pharmacy benefit manager shall not discriminate against a nonaffiliated pharmacy that is a  
retail pharmacy.  
MPA suggests that addi�onal details be listed in the rules regarding what “discrimina�on” classifies.  
Specifically, we ask that the following language be included.  
PBM’s duty includes not discrimina�ng against a nonaffiliated retail pharmacy that wishes to  
join a PBM’s standard or preferred pharmacy network, provided that pharmacy is willing and  
able to abide by the terms and condi�ons for network par�cipa�on.  
PBMs may not reimburse an affiliated pharmacy more than an unaffiliated pharmacy that  
operates in the same network as the affiliated pharmacywhether standard or preferred.  
For a drug intended for administra�on by a prescriber, the PBM shall not require that a pa�ent  
receive the drug via distribu�on from a mail-order or any other affiliated pharmacy for  
subsequent transporta�on to the prescriber’s office prior to administra�on. Nor shall that PBM  
impose any monetary penal�es or price discrepancies between drugs accessed by a retail  
pharmacy and a mail-order or affiliated pharmacy.  
IV.  
Non-discriminaꢀon against nonaffiliated pharmacies  
Public Act 11, 2022  
Sec. 27. (1) For each drug that a pharmacy benefit manager establishes a maximum allowable cost, the  
pharmacy benefit manager shall do all of the following:  
(a) Provide each pharmacy subject to a maximum allowable cost list with access to the maximum allowable  
cost list and the source used to determine the maximum allowable cost for each drug.  
(b) Update its maximum allowable cost list at least once every 7 calendar days.  
(c) Provide a process for each pharmacy subject to the maximum allowable cost list to receive prompt  
noꢀficaꢀon of an update to the maximum allowable cost list.  
(d) Establish and maintain a reasonable administraꢀve appeals process to allow a pharmacy subject to the  
maximum allowable cost list or an agent of a pharmacy subject to the maximum allowable cost list to  
challenge the adjudicaꢀon of a pharmacy’s claim.  
(e) Invesꢀgate and resolve an appeal under this subsecꢀon within 14 calendar days aꢂer the pharmacy  
benefit manager receives the appeal. An appeal under this subsecꢀon must be submiꢁed to the pharmacy  
benefit manager not later than 45 calendar days aꢂer the date the pharmacy’s claim for reimbursement  
has been adjudicated.  
(f) Respond in wriꢀng to any appealing pharmacy or an appealing pharmacy’s agent not later than 30  
calendar days aꢂer receipt of an appeal if the pharmacy filed the appeal more than 10 calendar days aꢂer  
the date the pharmacy’s claim for reimbursement is adjudicated.  
(g) If an appeal is denied, provide the appealing pharmacy or the appealing pharmacy’s agent the naꢀonal  
drug code number available for purchase in this state at or below the appealed maximum allowable cost.  
(h) If an appeal is granted, permit the pharmacy to reverse and rebill the claim and all claims for the  
drug.MPA suggests that addi�onal details be listed in the rules regarding what “discrimina�on” classifies.  
Specifically, we ask that the following language be included.  
In addi�on to the stated regula�ons, MPA recommends further clarifica�on regarding “Maximum  
Allowable Cost Lists” or “MAC” list. We recommend the following language be added to the rules:  
“Maximum Allowable Cost List” means a lis�ng of drugs or other methodology used by a  
pharmacy benefits manager, directly or indirectly, seng the maximum allowable cost on which  
reimbursement payment to a pharmacy or pharmacist may be based for a generic drug, brand-  
name drug, biologic product, or other prescrip�on drug.  
“Maximum Allowable Cost List” includes without limita�on:  
o
o
o
o
o
o
o
o
(i) Average acquisi�on cost, including na�onal average drug acquisi�on cost;  
(ii) Average manufacturer price;  
(iii) Average wholesale price;  
(iv) Brand effec�ve rate or generic effec�ve rate;  
(v) Discount indexing.  
(vi) Federal upper limits;  
(vii) Wholesale acquisi�on cost; and  
(viii) Any other term that a pharmacy benefits manager or a healthcare insurer may use  
to establish reimbursement rates to a pharmacist or pharmacy for pharmacist services.  
Thank you again for the opportunity to provide comments on these rules. If you have any ques�ons or  
require clarifica�on regarding our remarks, please do not hesitate to reach out.  
Respecully submited,  
Eric Roath, PharmD, MBA  
Director of Government Affairs  
Michigan Pharmacists Associa�on  
(906) 282-8930  
;