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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
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    Debunking Myths About GLP-1 Medications

    February 16, 2026
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    The Future of Healthcare Consumerism

    January 22, 2026
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    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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    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

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Home Trends

What’s the NEJM Doing?

Restricting access to pre-publications?

Jay K Joshi by Jay K Joshi
April 22, 2024
in Trends
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ATTACHMENT DETAILS Whats-the-NEJM-Doing-scaled.jpg April 19, 2024 350 KB 1693 by 2560 pixels Original image: Whats-the-NEJM-Doing.jpg Edit Image Delete permanently Alt Text What's the NEJM Doing

Toa Heftiba

Dawn Peters, Director of Strategic Communications & Media Relations at NEJM Group, has communicated via email that news outlets primarily catering to physicians will no longer qualify for embargoed access, or restricting access to clinical studies for a time to those who have paid for the content in advance. This comes as a surprise to many journalists as they seek renewal of their media credentials with the journal. Already several reporters from prominent health media outlets were declined on the grounds that their publication predominantly targets clinicians and healthcare professionals.

While specific reasons for this policy adjustment were not elaborated upon, there have been significant transformations in medical publishing and within NEJM’s own publications since the inception of its embargoed access policy many years ago.

The parent company of the journal, NEJM Group, has expanded to encompass multiple journals available for subscription by physicians and clinical professionals. This expansion coincides with an increase in media outlets targeting medical professionals. A significant portion of these media outlets’ content consists of summaries of articles from the family of NEJM journals, often crafted to meet the comprehension needs of clinicians who have direct access to our resources.

NEJM has strategically established a network of journals that republish content from various sources, thereby broadening its reader base. This initiative seems aimed at enhancing revenue generation by directing readers towards its suite of associated publications or requiring upfront payment.

In other words, NEJM perceives any entity authoring content for a clinical audience as competition. Consequently, it appears to be limiting access to its primary publication from those competitors.

More to the point, NEJM appears to be limiting access in an effort to increase their market presence. It seems to be prioritizing market expansion over the transparent and critical flow of clinical information. This tactic seems primarily about preserving a journal’s image and enhancing a publisher’s brand. See maintaining a brand identity, which is an odd approach from a medical journal.

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Jay K Joshi

Jay K Joshi

Dr. Joshi is the founding editor of Daily Remedy.

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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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