10.22.26 -- Design For Contamination Control

Modern aseptic monitoring requires a shift from periodic checks to risk-based strategies. Learn how to integrate particle and environmental data to meet Annex 1 standards and ensure patient safety.

Particulate analysis and Container Closure Integrity Testing determine whether a pharmaceutical batch holds up under regulatory scrutiny, and why a single flawed reading can carry real consequences.

Gain insight into how a unique patient-centric formulation simplifies medication administration for patients of all ages, especially those with swallowing difficulties.

In this segment from the Pharmaceutical Online Live event, our panelists talk about designing the production space to minimize interventions, involving operators in design, selecting the right technology, and considerations for ready to use components versus bulk components.

Prepare for updates to IEC 62304 by learning how revised process rigor levels and expanded health software scopes impact medical device software development and compliance.

Flexible stick pack production supports powders, granules, and liquids while enabling faster changeovers. See how controls and digital connectivity help prepare packaging operations for Pharma 4.0.