As organizations change constantly, there is an increasing need to adopt agile, scalable resourcing models. This is especially relevant to the health science industry. Choosing a global supplier who can support operations through the provision of appropriately skilled resources, within regulated environments, allows your organization to remain agile, while avoiding…

ICH, EMA and FDA guidelines demand stress testing of all drug substances and drug products. In order to ensure compliance, you need accurate testing to confirm stability indicating analysis, establish potential forced degradation pathways and allow characterization of product-related impurities. We offer state-of-the-art laboratories and expert methodologies for forced degradation…

To help you meet ICH Q6B guidelines, you need accurate impurities and contaminants analysis in biotechnology products during product characterization. We offer a number of services and techniques providing impurities and contaminants characterization in biotechnology derived products. As a world-leading provider of impurities and contaminants analysis in biotechnology products, we…