We speak with Mr. JeVon McCormick, CEO of Scribe Media and author of Modern Leader. Mr. He helps individuals from ...
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We discuss trends in the comments that have appeared in response to the draft version of the updated clinical practice ...
Today we are here with Dr. Thomas Kline and Jonelle Elgaway, of the National Pain Council, a citizen's group with ...
We discuss the rise in retractions among academic publications, and the pandemic's impact on retractions in clinical journals over the ...
We discuss Dr. John Whyte's latest book, Take Control of Your Diabetes Risk, and reveal what it offers patients struggling ...
We discuss Miss Haelle's struggles to overcome vaccine misinformation during the pandemic. As a journalist, she often found herself at ...
We discuss Miss Lamb’s experiences during the pandemic and glean her thoughts on how it affected the quality of writing ...
We discuss her journalism as a writer and lived experiences as a patient during the pandemic, chronicling a timeline of ...
We discuss addiction policies in Rhode Island and demonstrate how bureaucracies can influence the passing of addiction policy and law. ...
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We discuss the oral arguments presented on March 1st in the seminal case, Ruan v. United States - arguably the ...
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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© 2026 Daily Remedy