Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
Meet Intertek at AusBiotech 2016, Australia’s Life Sciences Conference, October 24-26, Melbourne, AustraliaIntertek will be exhibiting and available for partnering meetings at AusBiotech 2016. Our experts in pharmaceutical analysis and large molecule bioanalysis will be present at Booth 65 to discuss all aspects of contract laboratory services and pharmaceutical and biopharmaceutical product characterisation services. In particular, the team can advise on strategic approaches to preclinical and clinical evaluation through LC-MS bioanalysis and immunogenicity assays, including cell-based neutralization assays, ligand-binding assays, method development and validation of bioanalytical methods, PK/PD bioanalysis for monoclonal antibodies and antibody-drug conjugates (ADCs) and the design of bioanalytical programs for biosimilar comparability. Our GMP team will be present to discuss your outsourcing needs for pharmaceutical analysis, extractables / leachables, GMP stability studies, analytical method development and validation.
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