Available on Demand

Packaging materials and designs have evolved and continue to do so exponentially, on par with the unique products they hold. As a result, manufacturers and suppliers find it challenging to adhere to regulatory requirements, best practices, and appropriate test standards.

This webinar will provide an extensive overview of container and package qualification across the product lifecycle. Our speaker, Brandon Zurawlow, CSO, CS Analytical, will review relevant and recently revised and pending USP chapters applicable to different packing materials and components.

The session will also cover critical evaluations referenced in regulatory guidance and best practices, compendial and non-compendial standards, and case studies of product-package systems.

Learning Objectives

• Explore the FDA guidance and regulatory requirements for pharmaceutical container and package systems.
• Learn how compendial test procedures fit into the broader container qualification framework.
• Note the relevant non-compendial evaluations for packaging systems that ensure successful regulatory compliance.