Defining the context of use helps ensuring that biomarker assays are developed, validated and applied in a manner that meets the specific needs and goals of the research or clinical application. It provides a framework for evaluating the assay’s performance and suitability, which can ultimately lead to more reliable and meaningful biomarker data. Based on the context of use, our experts not only suggest a suitable platform and assay type but also guide you through the fit-for-purpose validation setup.
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By leveraging the specificity of antigen-antibody interactions, immunoassays enable precise detection of a wide array of biomolecules. Various platforms for ligand binding assays are available at Nuvisan, offering the flexibility to support biomarker projects individually.
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Liquid chromatography-mass spectrometry (LC-MS) is a highly sensitive and specific analytical technique widely used for the analysis of a diverse range of biomarkers. Its ability to separate complex mixtures and identify compounds based on their mass-to-charge ratio makes it an invaluable tool.
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Located alongside our Clinical Pharmacology Unit (CPU), our clinical laboratory is committed to delivering highest-quality data and insights to not only support safety assessments but also pharmacodynamic biomarkers.
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Nuvisan’s own isochronic library was set up to support your biomarker stability assessment and help save you valuable time during assay validation.
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