The core principle of BETMAT’s Kinetic Chromogenic LAL Assay is based on the specific enzymatic cascade triggered by the interaction between Limulus Amebocyte Lysate (LAL) and bacterial ...

What makes sterile medications different from other types of prescriptions? Compounding pharmacist Corey Dolan of Preckshot ...

The buying on the counter came after the company received World Health Organization (WHO) prequalification approval for ...

Pharmaceutical labeling is becoming a dynamic, safety-driven process that supports both regulatory needs and patient care. Updated USP standards and global compliance requirements are pushing ...

The growing complexity of the field reinforces the need for standards ensuring product quality, consistency, and patient ...

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Concurrent IRA and MFN pricing mechanisms are compressing margins and reshaping R&D, investment, and manufacturing decisions, with expectations that these pressures will persist and broaden in scope.

HPLC, ICP-MS, GC-MS, and LC-MS/MS testing with ICH Q2(R1)-validated methods, 48-hour turnaround, and pharma-grade documentation for supplements and FBA sellers ...

· By creating clear compendial pathways for digital standards and methods, USP hopes to reduce uncertainty and help manufacturers adopt emerging technologies with greater confidence. · Enhanced ...

Anthony Lakavage, executive vice president and head of Global External Affairs at USP, talks about how sustainability efforts are more than just protecting the environment and how pharmaceopeias are ...

Polymer-based excipients, including lactide-glycolide and lactic acid-glycolic acid polymers (PLGs and PLGAs, collectively referred to as LG polymers), play a vital role in enhancing controlled drug ...

USP Chapter 797 outlines new compliance guidelines for Category 2 and Category 3 compounding, including more comprehensive documentation requirements, more frequent competency verification, and ...