Pharma
How GLP-1 Drugs Are Reshaping Anesthesia Practice

How GLP-1 Drugs Are Reshaping Anesthesia Practice

Few classes of medications have changed the perioperative conversation as quickly as glucagon-like peptide-1 receptor agonists (GLP-1 RAs). Originally developed primarily for the management of type 2 diabetes, GLP-1 therapy is now widely used for obesity and metabolic...

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Why Pharmaceutical Quality Cannot Be Tested Into a Product

Why Pharmaceutical Quality Cannot Be Tested Into a Product

In pharmaceutical manufacturing, quality control testing is often the point at which a product gets its final analytical assessment. But from my experience in pharmaceutical quality control, one principle is worth emphasizing: QC testing is essential, but QC testing...

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Semaglutide Patent Expiry: What Generics Did to Prices

Semaglutide Patent Expiry: What Generics Did to Prices

The semaglutide patent expiry of March 2026 has now had six months to work. The evidence is uneven. In India, prices fell by up to 70% within weeks. In Canada, generic pens reached pharmacies in May. In China, not one generic has been approved. Readers in the United...

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Foundayo vs Rybelsus: The Oral GLP-1 Guide for 2026

Foundayo vs Rybelsus: The Oral GLP-1 Guide for 2026

The oral GLP-1 market has changed faster in the past six months than in the previous six years. Where once Rybelsus stood alone as the only GLP-1 pill available, patients and clinicians must now navigate three distinct oral products, each with a different molecule, a...

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The GLP-1 Drug Pipeline: Every Candidate to Watch in 2026

The GLP-1 Drug Pipeline: Every Candidate to Watch in 2026

The GLP-1 drug pipeline has become one of the most consequential and closely watched in modern pharmaceutical history. In 2026, the class of glucagon-like peptide-1 receptor agonists is no longer defined solely by Ozempic and Wegovy. A new generation of oral tablets,...

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PDUFA Date Explained: FDA Drug Approval Deadlines

PDUFA Date Explained: FDA Drug Approval Deadlines

Every time a pharmaceutical company submits a new drug to the US Food and Drug Administration, a clock starts. That clock ends on the PDUFA date. For anyone working in life sciences, whether in regulatory affairs, clinical research, investment, or commercial planning,...

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