Compendial Testing (USP/BP/EP/JP, Other)

Compendial Testing (USP/BP/EP/JP, Other)

We specialize in compendial monograph and pharmacopoeial testing services to ensure the identity, strength, quality, and purity of your pharmaceutical materials. Utilizing standardized methods from the USP-NF, EP, JP, BP, and other international pharmacopeias, we analyze APIs, excipients, intermediates, and finished products while providing a certificate of analysis (C of A) under our cGMP-compliant operations. Our services include physical and chemical testing, such as dissolution studies, residual solvent analysis, metals analyses, spectrophotometry, pH measurements, and impurity identification, among others. Recognizing that some projects require alternative methods, we also offer method development and validation to meet ICH, USP, and EP regulatory guidelines. With our FDA-inspected, DEA-licensed facilities and experienced team, we provide precise, reliable results and consultation services to help you confidently meet your regulatory submissions and manufacturing quality objectives.