Saturday, May 23, 2026
ISSN 2765-8767
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A conversation on health policy and misinformation with Dr. Josh Bloom of ACSH

Dr. Jonathan (Josh) Bloom, ACSH’s Director of Chemical and Pharmaceutical Science, earned his Ph.D. in organic chemistry at the University of Virginia, followed by postdoctoral training at the University of Pennsylvania. His first career was in drug discovery research, mostly at Wyeth. During this time he participated in research in a number of therapeutic areas, including diabetes and obesity, new antibiotics, HIV/AIDS, and hepatitis C. His group discovered the novel antibiotic Tygacil®, which was approved by the FDA for use against resistant bacterial infections in 2005. He is the author of 25 patents, and 35 academic papers, including a chapter on new therapies for hepatitis C in Burger’s Medicinal Chemistry, Drug Discovery, and Development, 7th Edition (Wiley, 2010). Dr. Bloom joined the American Council on Science and Health in 2010 as Director of Chemical and Pharmaceutical Sciences.

The articles featured are:

DEA Chasing Its Tail Again: This Time, It’s ‘Synthetic Cannabinoids’

DEA Chasing Its Tail Again: This Time, It’s ‘Synthetic Cannabinoids’

Tylenol Plus Advil Combo: Innovation Or Exploitation?

Tylenol Plus Advil Combo: Innovation Or Exploitation?

Daily Remedy

Daily Remedy

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.

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Videos

Policy Shift in Peptide Regulation

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

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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