TGA BioServices (FDA/EMA registered and inspected) provides GLP, GCLP, and cGMP regulatory-compliant services for RUO, pre-clinical toxicity studies, clinical trials, and batch release testing. We offer dedicated QA/QC personnel to insure compliance to required guidelines and the highest quality of the data.

Our team has many years of experience in the development and validation of immunoassays for compound screening, ADA, Nab, PK, biomarkers testing using variety of methodologies. We provide the white gloves service covering all aspect of your bioanalytical needs from preparing the sample collection kits and training the clinical sites for proper specimen’s management to creating a FDA ready Validation and/or Sample Analysis Reports.

We value a close relationship and communication with our clients, you’ll always have a dedicated team who’ll answer your questions within 24 hours and you will know in real time what is going on with your study including any budget updates.

Core Expertise and Technology: