
Effective drug development requires accurate testing, specialized support and precise results. From preclinical to early and late clinical phases, we provide comprehensive bioanalytical solutions for your drug development.
With over 30 years of experience, operating out of our GLP/GCP compliant laboratories, we provide expertise to develop assays from scratch. We also support large-scale routine sample analyses – from regulatory pre-clinical (toxicology) to early and late clinical studies (Phase I to IV). We have also recently gained enhanced testing capabilities with advanced ELISA equipment and the Gyrolab xPlore system.
Small molecules, biologics, biosimilars and biomarkers
Small molecules, biologics and biosimilars
Soluble and cellular biomarkers
Screening, confirmatory, titration characterization and neutralizing antidrug antibody assays
Parent drug, metabolites, and biomarkers
LBA/LC-MS/MS:

We are the world’s leading inspection, verification, testing and certification company. In addition to our bioanalytical solutions, we offer industry-leading contract development and manufacturing (CDMO), and analytical development and testing.
We support you every step of the way to enable you to deliver first-class, fully compliant biopharmaceutical and pharmaceutical drugs, clinical research, and medical devices.
To discuss your bioanalytical requirements, contact us today.