Identifying the Right Investigators and Patients for your Study – Mini Podcast Biosimilar Development Capabilities – Watch Now Vaccine Development Capabilities - Brochure Check out our latest Validated PK & ADA Methods List Read about Veeda's partnership with Ahammune Biosciences for first in human studies Check out our Assay List (Method Library)

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

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PK/PD and Immunogenicity Testing with Advanced Bioanalytical Platforms

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Veeda Biopharma offer 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

  • Quantify Free/Bound/Total drug concentrations in biological matrices
  • Incurred Sample Reanalysis
  • Statistical Analysis
  • Biomarker Estimations
  • Neutralizing Antibody (NAb) Detection - Cell-Based or Competitive Ligand Binding (CLB) Assays
  • Analysis of Anti-Drug Antibodies (ADAs) Using Tier Based Approach
    • Screening
    • Confirmatory
    • Titer

Biotherapeutics

Pharmacokinetics

Pharmacodynamics

Immunogenicity

Your GIF

Accelerate Your Vaccine Program with Reliable, High Quality Immunogenicity Testing

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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

Maximizing Assay Accuracy and Consistency through Advanced Critical Reagent Development

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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

Affinity

Labelling of
Critical Reagents

Qualification &
Optimization

Achieving Regulatory Excellence Through Global Quality Standards and GCLP Compliance

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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

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BioTek Synergy H1

QuickPlex SQ 120

AB SCIEX QTRAP 6500+