You can rely on Cerba Research to outsource your research questions, including efficacy, safety, passive immunization, immunogenicity, pharmaco kinetics, pathogenicity, antiviral therapy, antiviral prophylaxis, drug delivery, resistance mutants, and more.

With more than 4500m2 clinical laboratories, equipped with the latest technologies, we have the in-house capabilities to perform several read outs. We are experts on evaluation of immune responses, antibody detection, vaccine efficacy; immunogenicity, pharmaco kinetics, immunopathology, antiviral therapy, antiviral prophylaxis and more. Our portfolio of immunological assays include: Haemagglutination inhibition, Neutralizing antibodies, Neuraminidase inhibition, cell mediated immunity and immunogenicity testing.

Cutting-Edge Platforms

To support the development, validation, and implementation of our immunoassays, we employ the most advanced platforms in the industry. Our expertise extends to ELISA, MSD, ELLA, and Luminex, ensuring optimal performance and reproducibility for every project. Our off-the-shelf 37-plex MSD panel is currently in high usage within many of our trials.

Clinical value of our 37-plex MSD panel: Many diseases are characterized by inflammatory processes. Cytokines, as mediators of inflammation, may serve as biomarkers to characterize disease progression and therapy response. The 37-plex MSD panel is also relevant for cytokine release syndrome (CRS) safety assessment which is useful for cell & gene therapy trials.

Customized Immunoassay Test Solutions

If we don’t have it, we can customize it. We understand that each research project is unique, requiring tailored immunoassay test solutions. Our experienced scientists work closely with you to design and optimize assays tailored specific to your research needs. We offer flexible options to accommodate various sample types.

Quality Assurance and Regulatory Compliance

Delivering reliable and high-quality data is our utmost priority. Cerba research diagnostic laboratory has adopted a high-quality standard in all operations, testing procedures and reporting. The quality management system is based on ISO 15189, GLP, GCLP, GSLP, and expanded with elements of GCP, to comply with regulatory requirements and facilitate regulatory submissions. Our commitment to quality ensures that your research findings are robust, reliable, and ready for further development.