Thermo Fisher Scientific Expands Steriles Manufacturing and Research Capabilities in Asia-Pacific Region
There is a common view among biopharmaceutical regulatory agencies that process validation is requirement for all commercial products. These activities are a critical component in protecting patients by minimizing risk and ensuring product quality throughout a product’s life cycle. Manufacturers have a wide variety of options to choose from when constructing a process validation strategy – including the specific process characterization approaches needed to define a well understood and controlled commercial manufacturing process.
Listen to our on-demand webinar, hosted by France Biotech with Thermo Fisher expert Daniel Baskind, to learn more about this important topic.