Dr. Jay K Joshi serves as the editor-in-chief of Daily Remedy. He is a serial entrepreneur and sought after thought-leader for matters related to healthcare innovation and medical jurisprudence.
He has published articles on a variety of healthcare topics in both peer-reviewed journals and trade publications. His legal writings include amicus curiae briefs prepared for prominent federal healthcare cases.
Behavioral intervention has limited benefits because it doesn't address how patients think about their clinical decisions.
The CDC unveiled its latest opioid prescribing guidelines. It's decidedly more patient centric, but fails to account for how law...
Enough time has passed to where we are reflecting on the pandemic for a sense of closure. We would be...
Medicare Advantage plans are facing scrutiny after years of excessive billing practices. The fraud exemplifies how delivery models cannot align...
HIPAA was designed to protect patient rights. But for victims of gun violence and the advocates who help them, it...
Journalists often portray gun violence through familiar patterns of writing. This format misrepresents the full story of those involved.
Gun violence data may appear startling, but they lack meaningful context. It would help to correlate the statistics with broader...
The FDA has asked the DOJ for support in issuing its first ever injunction against six vaping manufacturers.
Viruses are acting differently. It's clear the pandemic altered the virosphere in unknown ways, with consequences yet to emerge.
Venture capital firms are pouring lavish sums into environmental health. Will there be a return on investment?
Many physicians have become social media influencers. Their online presence has altered the patient relationship in ways we have yet...
We're familiar with online misinformation. But we’re less familiar with how information overload affects our judgment. It’s time to study...
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