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Analytik Jena Opens €96 Million German Facilities to Expand Laboratory Instrumentation Capacity

Analytik Jena opens €96M German facilities, expanding lab instrumentation output that could ease procurement pressure for pharma QC labs.

FDA Establishes CDER Exclusivity Board to Standardize NCE and Biologic Exclusivity Rulings

CDER's new Exclusivity Board will oversee NCE, new clinical trial, and biologic exclusivity determinations to improve consistency across rulings.

Alcon Gains FDA Approval for Brytly, First Nonprescription Apraclonidine Eye Drop

Alcon's Brytly becomes the first nonprescription apraclonidine eye drop approved by FDA, signaling continued agency push on OTC drug access.

FDA Flags Bacterial Contamination Risk in Counterfeit DLC Laboratories and ProMex Eye Drops Across Six States

FDA confirms bacterial contamination in counterfeit eye drops from DLC Laboratories, ProMex, and Laboratorios Sophia found across six U.S. states.

EMA CHMP Grants Six Positive Opinions in October 2026, Including Oral GLP-1 Orforglipron and Two Biosimilars

EMA's CHMP issued six positive opinions in October 2026, including oral GLP-1 orforglipron and two biosimilars, with key implications for EU market entry.

Adial Pharmaceuticals Appoints David Rubenstein as Chief Scientist

Adial Pharmaceuticals names tapinarof architect David Rubenstein as Chief Scientist to lead AT177 through IND-enabling studies toward 2027 first-in-human trials.

Dermata Reports Positive Results from Tome Skincare Study

Dermata Therapeutics reports topline cosmetic study data for Tome Foundational Treatment, with 71% of participants showing improvement after one application.