We take pride in our ability to develop modern sample preparation techniques for separating analytes and metabolites from plasma, serum, blood, and other biological matrices for detection and quantification, as well as in validating methods in full compliance with current regulatory guidelines, and GLP requirements.

Our team are highly experienced with expertise in small and large molecules and its metabolites along with peptides, hormones, steroids, and other endogenous compounds.Our method development capabilities include sensitive and reliable bio analytical methods for generics and New Chemical Entities (NCE). We have expertise in challenging methods, such as those requiring drug derivatization, chiral separation and multiple metabolite quantitation.

We use the most advanced technologies and strategies to ensure on-time delivery of high-quality data. Our bioanalytical laboratory is equipped with state-of-the-art instruments and automated systems to conduct a wide range of analyses on biological samples. Our SOPs fully comply with Good Laboratory Practices (GLP) and are regularly reviewed and updated to align with evolving international regulatory standards and industry expectations.

With deep expertise in LC-MS/MS instrumentation and applications, our highly qualified scientific team ensures efficient method development and validation as per global regulatory requirements and client needs. We also provide a library of validated methods across major therapeutic areas, enabling rapid turnaround for drug and metabolite analysis in biological fluids.