We bring decades of experience and deep regulatory knowledge to biosimilar testing. Our team of bioanalytical experts specializes in product characterization, pharmacokinetics (PK), and immunogenicity for both originator biologics and biosimilars.
From early discovery through Phase III clinical trials and beyond, we provide the data and insights you need to move your biosimilar forward with confidence.
We support biosimilar development across a wide range of biologic drug classes, including:
Monoclonal antibodies
Metabolic hormones
Immunomodulatory drugs such as Trastuzumab, Bevacizumab, Cetuximab, and Adalimumab
Our tailored bioanalytical and characterization packages are designed to meet the unique requirements of your biosimilar program, in full alignment with FDA and EMA regulatory guidance.
Using the latest instrumentation and validated procedures, we deliver high-quality, reproducible data that meets global regulatory standards. Our capabilities include:
Immunogenicity and PK studies
Biomarker analysis
Cell-based assays
Assay development, validation, and transfer
Whether you're developing new assays or transferring existing methods, we ensure accuracy, compliance, and timely delivery of critical data.
No two biosimilars are alike—and neither are their testing requirements. Our philosophy is rooted in flexibility and scientific rigor. We understand the complexities of biosimilar comparability and offer customized solutions to address your specific challenges.
With extensive experience in biologics and biosimilars, we help you:
Design and validate fit-for-purpose assays
Navigate regulatory pathways with confidence
Generate robust data for comparability and immunogenicity assessments