11.20.25 -- Optimize Formulation And Integrity Workflows

Explore five areas that can form part of a QRM strategy to ensure the compliant manufacturing of sterile drug products: PUPSIT in a contamination control strategy, reducing human error and the evolution of training, assuring single-use system integrity, when to perform filter validation, and filter integrity test instruments.

Single-use technologies are transforming the way biomanufacturers approach production from upstream processing to final fill. Examine the key stages of implementation and how strategic choices drive success across the entire production process.

Maintaining the integrity of single-use systems is critical to contamination control, especially as manufacturing environments become more complex and regulatory expectations continue to evolve. See how a holistic approach to single-use system integrity can strengthen contamination control and improve operational efficiency.