We provide comprehensive analytical method development and validation services for pharmaceutical companies and testing laboratories. Our expertise covers HPLC, UHPLC, LC-MS/MS, GC-MS, dissolution testing, and other analytical techniques. Services include method development from scratch, method optimization, forced degradation studies, and complete ICH-compliant validation protocols.
Our analytical scientists work closely with clients to develop stability-indicating methods, impurity methods, and bioanalytical methods meeting regulatory requirements. We also offer method transfer services, ensuring successful implementation of analytical methods across different laboratories. All methods are developed with regulatory compliance in mind, supporting FDA, EMA, and other global regulatory submissions.