07.31.25 -- STREAM Edition: Designing For Future Flexibility And Adaptability

Delve into the intricacies of combination products and the regulatory expectations, including risk-based determination, evaluation, and documentation approaches for performance requirements.

In this Pharmaceutical Online Live event, “Facility Design And Validation Considerations For Drug Manufacturers,” our panelists respond to an audience question about designing a facility with future needs in mind.

Discover how MSD ensures continuous inspection readiness with digital validation and ALCOA+ principles to drive compliance, data integrity, and streamlined automation.

Examine essential analytical techniques in biotherapeutics development, as well as explore ITC, DSC, and Rheology—powerful tools for understanding formulation, stability, and efficacy in drug development.

Explore challenges QA professionals face in document reviews and expert strategies to boost accuracy, streamline workflows, and ensure compliance with evolving regulatory standards.

Uncover a cutting-edge, non-destructive method for container closure integrity testing using CO₂ tracer gas and headspace analysis—an advanced alternative to traditional dye ingress techniques.