Clinical Bioanalysis

Veeda Biopharma offers comprehensive large-molecule bioanalytical services for both early and late-phase clinical trials. We deliver precise data using advanced technology and strict quality assurance, adhering to GCP and GLP standards. Our expertise ensures accurate, efficient analysis, empowering informed decisions for successful biotherapeutic development.

Clinical Bioanalysis Service by Veeda Lifesciences

PK/PD and Immunogenicity Testing with Advanced Bioanalytical Platforms

Veeda Biopharma offers clinical bioanalysis services for method development, validation, and sample analysis using state-of-the-art LC-MS/MS and Ligand Binding Assay platforms (ELISA and ECL) for bioanalysis of biotherapeutics, meeting the needs of clients involved in drug development and regulatory submissions utilizing robust, sensitive, specific and reproducible methods.

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Quantify Free/Bound/Total
Drug Concentrations in Biological Matrices

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Analysis of Anti-Drug Antibodies (ADAs)
Using Tier-Based Approach
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Screening

Confirmatory

Titer

Antibody Icon

Neutralizing Antibody (NAb)
Detection – Cell-Based or
Competitive Ligand Binding (CLB) Assays

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Biomarker
Estimations

Accelerate Your Vaccine Program with Reliable &
High-Quality Immunogenicity Testing

Veeda Biopharma accelerates vaccine development with rapid, high-quality immunogenicity testing for bacterial and viral vaccines. Our innovative immuno-analytical methods ensure precise results, focusing on humoral and cell-mediated immune responses, helping you achieve the highest scientific standards for your vaccine programs.

Veeda Lifesciences offers a comprehensive suite of bioanalytical assays for Generics, New Chemical Entities (NCEs), Biotherapeutics. Our services include custom assay development, validation and sample analysis for small molecules and large molecules, with focus on pharmacokinetics (PK), pharmacodynamics (PD), immunogenicity testing and biomarker analysis. Leveraging advanced ligand-binding platforms and mass spectrometry technologies, we ensure high-quality and precise results. Our assays support all stages of drug development, including biosimilar development, ensuring regulatory compliance and the highest scientific standards.

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Maximizing Assay Accuracy and Consistency through Advanced Critical Reagent Development

We offer specialized critical reagent development services to ensure the accuracy and consistency of your Ligand Binding Assays. By leveraging advanced characterization techniques, we optimize reagents for specificity, affinity, stability, and purity, enabling precise and reproducible measurements of target analytes in biological samples.

Generation

Purification

Labelling of Critical Reagents

Qualification

Clinical bioanalysis expert using a tablet with advanced technology icons, representing precision healthcare

Achieving Regulatory Excellence Through Global Quality Standards and GCLP Compliance

Clinical Bioanalysis team utilizes a robust Quality Management System (QMS) to ensure the highest quality data at every stage of analysis, providing the accountability and traceability necessary for regulatory submissions. Our bioanalytical services are conducted in GCLP-compliant laboratories, adhering to stringent regulatory guidelines from ICH, FDA, EMA, and current industry whitepapers.

State-of-the-Art Technologies

AB SCIEX QTRAP 6500+ Picture

AB SCIEX QTRAP 6500+

Picture of BioTek Synergy H1

BioTek Synergy H1

Picture of MSD QuickPlex SQ 120

MSD QuickPlex SQ 120