Bioanalytical

Platforms

At BioLegacy, our bioanalytical laboratory translates your biological samples into definitive, quantitative data for confident decision-making. Our multi-platform approach accurately measures drug concentrations, assesses immunogenicity, and quantifies key biomarkers. Leveraging a diverse and integrated suite of advanced technologies – including high-sensitivity Meso Scale Discovery and ELISA for protein analysis, multi-color flow cytometry for cellular characterization, and digital and real-time PCR for gene expression – we deliver a robust, data package that provides deep mechanistic insight and fully supports your program’s regulatory submissions.

  • Multi-Platform Ligand Binding Assays (LBAs): n various platforms, including ELISA and electrochemiluminescence (MSD), for PK, ADA, and biomarker analysis.
  • Advanced Cellular Analysis: via multi-color flow cytometry.
  • Gene Expression Analysis: and precise nucleic acid quantification using real-time (qPCR) and digital PCR (dPCR).
  • GLP-Compliant Bioanalysis: Dedicated, GLP-compliant laboratory and Quality Assurance unit
  • Support for a Broad Range of Modalities: Small molecules, large molecules, ADCs, targeted protein degraders (TPDs), cell and gene therapies, and others.
  • Full Method Lifecycle Support: from de novo method development and phase-appropriate validation to GLP testing for IND-enabling studies.
  • Integrated PK/PD & TK Analysis: Rapid sample turnaround and expert interpretation.
  • Immunogenicity & Anti-Drug Antibody (ADA) Testing: Screening, confirmatory, and neutralizing antibody assays.
  • Comprehensive Biomarker Services: Discovery, validation, and quantitative analysis of soluble and cell-based pharmacodynamic and safety biomarkers.
Small Molecule Bioanalysis

Precise quantification of drug and metabolite concentrations is the cornerstone of pharmacokinetic and toxicokinetic analysis. Our small molecule bioanalysis platform is built around state-of-the-art liquid chromatography-tandem mass spectrometry (LC-MS/MS). This technology provides the ultimate sensitivity and specificity required to accurately measure compound levels in a wide variety of complex biological matrices, delivering the definitive exposure data needed to interpret your in vivo studies.

  • High-sensitivity: LC-MS/MS instrumentation
  • Pharmacokinetic (PK): & Toxicokinetic (TK) analysis
  • Metabolite: identification and quantification
  • Method development: validation, and transfer
  • Analysis: from a wide range of biological matrices
Large Molecule Bioanalysis

BioLegacy provides comprehensive support for analysis of biologics through a diverse portfolio of ligand binding assays (LBAs). By leveraging the high sensitivity and broad dynamic range of our ELISA and Meso Scale Discovery (MSD) electrochemiluminescence platforms, we robustly quantify therapeutic proteins and assess critical immunogenicity, providing key data for your IND submission.

  • High-sensitivity: protein quantification (PK)
  • Anti-Drug: Antibody (ADA) & immunogenicity testing
  • Neutralizing: Antibody (NAb) assays
  • Soluble biomarker: and cytokine profiling
  • Support for mAbs: ADCs, peptides, and vaccines

Cellular & Molecular Biology Platforms

Understanding a therapeutic’s mechanism of action often requires interrogating its effects at the cellular and molecular level. BioLegacy’s advanced platforms provide these deeper mechanistic insights. We utilize multi-color flow cytometry for detailed immunophenotyping and cellular biomarker analysis, alongside real-time and digital PCR for precise quantification of target gene expression, delivering a clear picture of your compound’s biological activity.

  • Multi-color: flow cytometry for cellular target engagement
  • Receptor occupancy: and immunophenotyping
  • Quantitative gene: expression analysis (qPCR/dPCR)
  • Biodistribution studies: for cell and gene therapies
  • Validation: of pharmacodynamic (PD) biomarkers

GLP Analysis for IND-Enabling Studies

All our bioanalytical services can be performed in a rigorously controlled, GLP-compliant environment to support your IND-enabling studies. Our laboratory operations are governed by a robust quality management system and overseen by an independent Quality Assurance Unit. BioLegacy’s commitment to data integrity, traceability, and regulatory compliance ensures that we deliver an unimpeachable data package ready for global regulatory submissions. Datasets in Standard for Exchange of Nonclinical Data (SEND) format are also available upon request.

  • GLP-compliant: laboratory environment
  • Phase-appropriate method: validation (ICH M10)
  • Independent Quality Assurance: Unit (QAU) oversight
  • 21 CFR Part: 11-compliant data systems
  • Optional: SEND data packages
  • Proven track record: in supporting regulatory filings
The tool is only as good as the operator. Trust the experts.
  • Deep analytical experience
  • The latest analytical technologies
  • Support for all therapeutic modalities
  • ICH GCP compliance for IND-enabling studies
  • Rapid study turnaround
Get the data you need. Contact us today.