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Intertek, in business more than 130 years with 42,000+ people in over 100 countries, has 25+ years of experience in regulated bioanalytical studies supporting the development of pharmaceuticals, biopharmaceuticals, vaccines and biosimilars through our global network of GCP/GLP compliant laboratories. We ensure products meet quality, health, environmental, safety, and social accountability standards for virtually any market. Our expertise in overcoming regulatory, market, and supply chain hurdles is unrivaled. Bioanalytical services include BA/BE, PK, ADA, Nab, ADC, immunogenicity, and LC-MS assays. Intertek’s ECL platform is applied to validation and qualification of quantitative biomarker assays and MSD panels in a variety of clinical matrices.