Company secures $5M in funding to accelerate its rapid testing platform USP<1223> Validation achieved, reinforcing 20-hour testing method Faster test results replace the standard 14-day USP sterility ...

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 ...

Comprehensive guide on ICH Q1A(R2) storage conditions, testing intervals, stability data for IND/NDA submission, and designing FDA-compliant stability programs ...

In 2010 the United States Pharmacopeia (USP) began modernizing their monographs [1]. As a part of this effort, test methods for the quantification of potassium now include ion chromatography. Ion ...