Webinar
A Quality-by-Design Approach to Annex 1 and Parenteral Packaging Manufacturing and Supply
Explore how a QbD-driven approach to parenteral packaging manufacturing supports compliance with EU GMP Annex 1 and builds a stronger foundation for sterile drug product quality.
Status
Published
Format
Webinar
Language
English
Access
Registration Required
Resource Overview
About this Webinar
The 2022 revision of EU GMP Annex 1 introduced significant new expectations for contamination control, manufacturing processes, and supplier oversight in sterile pharmaceutical manufacturing. In this webinar, Datwyler explores how Quality by Design (QbD) principles provide a structured framework for meeting—and exceeding—Annex 1 requirements, with a focus on how these principles apply to parenteral packaging component manufacturing and supply chain qualification.
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