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    How NADAC, WAC, and ASP Shape Drug Costs

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    March 22, 2026
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    Public Perception of Peptide Regulation and Compounding Practices

    Public Perception of Peptide Regulation and Compounding Practices

    April 19, 2026
    Understanding of Clinical Evidence in Peptide and Hormone Use

    Understanding of Clinical Evidence in Peptide and Hormone Use

    March 30, 2026

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    How NADAC, WAC, and ASP Shape Drug Costs

    How NADAC, WAC, and ASP Shape Drug Costs

    April 20, 2026
    The Hidden Costs Employers Don’t See in Traditional Health Plans

    The Hidden Costs Employers Don’t See in Traditional Health Plans

    March 22, 2026
    The Impact of COVID-19 on Patient Trust

    The Impact of COVID-19 on Patient Trust

    March 3, 2026
    Debunking Myths About GLP-1 Medications

    Debunking Myths About GLP-1 Medications

    February 16, 2026
    The Future of LLMs in Healthcare

    The Future of LLMs in Healthcare

    January 26, 2026
    The Future of Healthcare Consumerism

    The Future of Healthcare Consumerism

    January 22, 2026
  • Surveys

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    Public Perception of Peptide Regulation and Compounding Practices

    Public Perception of Peptide Regulation and Compounding Practices

    April 19, 2026
    Understanding of Clinical Evidence in Peptide and Hormone Use

    Understanding of Clinical Evidence in Peptide and Hormone Use

    March 30, 2026

    Survey Results

    Can you tell when your provider does not trust you?

    Can you tell when your provider does not trust you?

    January 18, 2026
    Do you believe national polls on health issues are accurate

    National health polls: trust in healthcare system accuracy?

    May 8, 2024
    Which health policy issues matter the most to Republican voters in the primaries?

    Which health policy issues matter the most to Republican voters in the primaries?

    May 14, 2024
    How strongly do you believe that you can tell when your provider does not trust you?

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Home Politics & Law

ERISA Preemption: The Legal Architecture That Protects Employers From States — and Sometimes From Accountability

ERISA preemption of state health insurance regulation was designed to allow multistate employers to operate uniform benefit plans. It has become, incidentally, one of the most powerful shields for pharmaceutical and insurance industry practices that states are eager to regulate.

Edebwe Thomas by Edebwe Thomas
May 21, 2026
in Politics & Law
0

ERISA preemption is the legal concept that the health policy community loves to cite and rarely examines with sufficient care. The Employee Retirement Income Security Act of 1974 preempts state laws that “relate to” employee benefit plans — a phrase that courts have interpreted expansively, if inconsistently, to cover most state attempts to regulate the design and administration of self-insured employer health plans. The preemption was intended to serve a straightforward administrative purpose: a national employer operating in fifty states should not need to comply with fifty different sets of benefit mandates and plan design requirements. The practical effect, never fully anticipated by Congress, has been to create a large carve-out from state insurance regulation that covers the majority of commercially insured Americans.

What Preemption Actually Forecloses

The range of state reforms that ERISA preemption forecloses is extensive and includes many of the most actively debated health policy interventions of the past decade. State drug price transparency laws that apply to PBMs? Preempted as applied to self-insured ERISA plans, though enforceable against fully insured markets. State surprise billing laws enacted before the federal No Surprises Act? Similarly limited in scope. State network adequacy standards for pharmacy access? Applicable to fully insured plans but not to the self-insured majority. The pattern is consistent: ambitious state-level health reforms that target market practices in the commercial insurance sector reach only the fully insured segment, which is increasingly the smaller and less influential part of the commercial market.

This dynamic creates a bifurcated regulatory environment that is rarely fully appreciated outside the benefits law community. A midsize company in California that offers a fully insured plan is subject to the California Department of Insurance’s network adequacy standards, PBM transparency requirements, and various benefit mandates. A competing company of similar size that self-insures is subject to none of them. The regulatory distinction has nothing to do with the companies’ relative sophistication as health plan sponsors; it is an artifact of a plan funding choice that was originally motivated by cash flow management and actuarial risk tolerance.

The Strategic Use of Preemption

PBMs and health insurers have historically been sophisticated users of the ERISA preemption argument, invoking it to defeat state regulations that would impose transparency obligations, restrict formulary practices, or mandate benefit coverage standards that the commercial products do not currently include. The insurance industry’s lobbying apparatus has consistently opposed state-level PBM regulation by arguing that the regulated entities’ contracts with self-insured employers are ERISA plans and therefore preempted — an argument that is often correct, frequently overstated, and almost always effective in narrowing the reach of state legislation.

The federal legislative response to ERISA’s preemptive scope has been incremental and largely reactive. The No Surprises Act, the Consolidated Appropriations Act’s PBM disclosure requirements, and the ACA’s coverage mandates are all layered onto the ERISA framework rather than restructuring it. Congress has shown no appetite for revisiting the basic preemption architecture, which has been stable since the Supreme Court’s Pilot Life v. Dedeaux decision in 1987 established the broad reading that has governed ever since. The preemption framework is not going away; the question for employers and states is how to work within it effectively.

The Employer’s Dilemma

The preemption framework creates an ironic situation for employers who are nominal beneficiaries of it. ERISA preemption protects employers from state mandates they might find burdensome, but it also insulates from state regulation the PBMs and other intermediaries whose practices may not serve employer interests. An employer in a state with aggressive PBM transparency requirements benefits from those requirements when it purchases a fully insured product but loses that benefit when it self-insures — which is when transparency matters most, because self-insurance puts the employer directly on the hook for drug costs. The legal architecture that gives employers flexibility in plan design also removes the state regulatory pressure that might discipline the intermediaries managing their benefits. It is a tradeoff that the original ERISA drafters did not contemplate and that the current Congress has not resolved.

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Edebwe Thomas

Edebwe Thomas

Edebwe Thomas explores the dynamic relationship between science, health, and society through insightful, accessible storytelling.

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Videos

summary

An in-depth exploration of drug pricing, including key databases like NADAC, WAC, and ASP, and how they influence the pharmaceutical supply chain, policy, and patient advocacy. The episode also introduces MedPricer's innovative pricing intelligence platform, offering valuable insights for healthcare professionals, policymakers, and patients.

Chapters

00:00 Understanding Drug Pricing Dynamics
03:52 Exploring the Drug Pricing Database
10:07 Patient Advocacy and Drug Pricing
13:56 Market Intelligence in Drug Pricing
How NADAC, WAC, and ASP Shape Drug CostsDaily Remedy
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Policy Shift in Peptide Regulation

Clinical Reads

FDA Evaluation of Certain Bulk Drug Substances in Compounding: Clinical Interpretation

FDA Evaluation of Certain Bulk Drug Substances in Compounding: Clinical Interpretation

by Daily Remedy
April 19, 2026
0

Clinicians increasingly encounter patients using or requesting peptide-based therapies sourced through compounding pharmacies. The U.S. Food and Drug Administration has identified a subset of bulk drug substances, including certain peptides, that may present significant safety risks when used in compounded formulations. The clinical question is whether these regulatory signals reflect meaningful patient-level risk and how they should influence prescribing behavior. This matters because compounded peptides often sit outside traditional approval pathways, creating uncertainty around quality, dosing consistency, and safety. Understanding...

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