Quality consistency is of paramount importance in the biopharma industry. It ensures the reliable development and manufacturing of safe and effective medications that meet stringent regulatory standards worldwide. At Thermo Fisher Scientific, this commitment to quality is embedded in every facet of our operations. We have implemented harmonized quality systems across all sites in our global network, ensuring that each location complies with country- and region-specific regulations, as well as our rigorous global quality standards.
We maintain high-level quality standards throughout drug development, from research and development to manufacturing. Our strategic initiatives include globally tracked risk and performance monitoring systems that enable us to identify and address potential issues proactively. Additionally, our site-specific maturity plans allow us to achieve quality objectives and promote continual improvement. This approach is complemented by our investment in a diverse pool of talent that actively promotes a strong culture of quality.
To learn more about our quality framework initiatives, tools, and methodologies, download our infographic.