Analysis service for samples

We offer services by developing various immunoassay methods related to efficacy parameters from human-derived specimens and clinical trial samples. We provide high levels of analytical services through an independent quality assurance system in accordance with clinical specimen analysis management standards and relevant regulations, covering all aspects of the analysis process including examination planning, execution, and reporting, ensuring reliability. We offer a wide range of analysis services, from efficacy evaluation of vaccines, including Human Papillomavirus (HPV) types 6, 11, 16, 18, 31, 33, 45, 52, and 58, to basic immunogenicity research.

Analysis items

We perform immune cell, antibody quantification, and neutralizing antibody analysis using the principles of absorbance or fluorescence measurement. We are capable of analyzing various cytokines, chemokines, and other biomolecules from serum, plasma, culture supernatant, cell lysates, and other clinical specimens.

Sampling and Management of Samples

We handle specimen sampling and storage management according to the client's requirements. We conduct sampling of clinical specimens (blood, plasma, serum, etc.) and cell culture under desired conditions, and provide specimen storage services under various storage conditions.

Follow-up management

During the commissioned period, Sponsor Audits are available to our clients. Additionally, we provide storage services for documents and specimens after the completion of the analysis, in accordance with the terms of the contract.