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The Transparency Paradox: Why Publishing Prices Can Raise Them
The case for hospital price transparency rests on a model of market competition that most hospital markets do not resemble....
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The Payer Mix Problem: Why Hospital Prices Mean Something Different Depending on Who’s Asking
A hospital's published negotiated rate for a hip replacement is not a price. It is a price-per-payer, averaged across the...
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Original Sourcing in Health Journalism Is Broken. Price Data Might Help.
───────────────────────────────────────────────────────── The sentence "a new study finds" has become health journalism's most reliable crutch—and its most dangerous one. There is...
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What Price Transparency Law Actually Produced—and What It Didn’t
The rule was written to empower patients. It has, instead, mostly empowered analysts. The CMS Hospital Price Transparency Rule, which...
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The Price Database That Reporters Keep Ignoring
Hospital price transparency was supposed to change everything—and in the newsrooms that cover health policy, it has changed almost nothing....
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Drug Pricing Transparency in an Era of Political Polarization: What MedPricer’s Data Reveals About a Contested Policy Landscape
Drug pricing data does not resolve policy debates—it sharpens them. When cross-benchmark analysis reveals that manufacturer list prices have increased...
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Pharmaceutical Data Licensing and the Institutional Market: Who Would Pay for MedPricer’s Dataset and Why
Data businesses in healthcare have historically underpriced their products relative to the value they generate, either because the buyers are...
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When Market Signals Are Ambiguous: The Interpretive Limits of Cross-Benchmark Drug Pricing Analysis
A widening spread between WAC and ASP is consistent with at least four distinct mechanisms: increasing PBM rebates for formulary...
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Medicaid Drug Rebates and the NADAC Baseline: What State Policy Makers Are Missing
Medicaid drug reimbursement policy is set by state agencies operating under federal minimum standards, with the specific details of dispensing...
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The Gross-to-Net Compression Dashboard in Practice: How Investors Would Actually Use It
The practical challenge for pharmaceutical equity analysts is not understanding the gross-to-net concept—it is getting systematic, time-series data that allows...
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The Generic Drug Supply Chain and What Pricing Benchmarks Reveal About Its Fragility
Generic drug shortages in the United States are a recurring feature of the pharmaceutical landscape—not anomalies but predictable consequences of...
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Physician-Executives and Drug Pricing Data: The Gap Between Clinical Awareness and Financial Literacy
The physician who becomes a health system chief executive brings clinical depth that is genuinely valuable in operational leadership—a capacity...
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FDA Evaluation of Certain Bulk Drug Substances in Compounding: Clinical Interpretation
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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The Importance of Access Control in the Workplace
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Drug Pricing Transparency in an Era of Political Polarization: What MedPricer’s Data Reveals About a Contested Policy Landscape
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Employer-Sponsored Insurance Is Breaking Down. Price Data Tells You Where It’s Happening First.
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Detecting Hospital M&A Synergies Before They’re Announced: A Rate-Based Event Strategy
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State Regulators and the Federal Data Gap: How MedPricer Fills What CMS Leaves Incomplete
