Practical steps for innovating pharmaceutical manufacturing

Innovation in pharmaceutical manufacturing is accelerating, driven by the need for greater efficiency, flexibility and product quality. As new technologies and materials are introduced, packaging systems and product-contact materials are playing an increasingly critical role in ensuring product safety and performance.

From single-use technologies to complex polymer-based container closure systems, manufacturers must carefully evaluate how materials interact with drug products. Extractables and leachables (E&L) have become a key consideration, with the potential to impact product stability, efficacy and regulatory compliance if not properly managed.

In this virtual panel, industry experts will share practical steps for advancing pharmaceutical manufacturing while embedding robust packaging strategies and E&L risk assessments into development and production. Attendees will gain insight into how a proactive, integrated approach can minimise risk, streamline approvals and support successful product lifecycle management.

Join this virtual panel to explore how to:

• Drive manufacturing innovation while maintaining control over product–packaging interactions
• Integrate extractables and leachables (E&L) assessments early in development
• Select and qualify packaging materials and container closure systems with confidence
• Address challenges associated with single-use systems and polymer components
• Align innovation strategies with regulatory expectations for E&L and packaging

Key learning points:

• Understand the growing importance of packaging in pharmaceutical manufacturing innovation
• Identify common sources of extractables and leachables across manufacturing and packaging systems
• Learn practical approaches to E&L study design and risk-based evaluation
• Explore how analytical testing supports material qualification and ongoing monitoring
• Discover strategies to ensure product quality, safety and compliance throughout the lifecycle

This panel is designed for professionals working at the sharp end of pharmaceutical manufacturing, including heads of operations and manufacturing, process development and engineering leads, quality and regulatory affairs directors, and senior professionals responsible for digital transformation. 

Be an early registrant, secure your spot now >>