The US Pharmacopeia’s Microbiology Expert Committee approved the inclusion of a chapter into the United States Pharmacopeia–National Formulary that allows the use of non-animal-derived reagents for ...
Pharmaceutical Technology® spoke with Nicola Reid, Associate Director Product Management, Endotoxin Products at Charles River Laboratories, to get her perspective on endotoxin testing and USP’s new ...
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 ...
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