Annex 1: How to Stay Ahead in Sterile Manufacturing

Adapting to Regulatory Changes and Enhancing Compliance in Aseptic Processing

Free Live Webinar

Date:  Wednesday, April 30th, 2025
Time:  5:00 PM AEST

Abstract

The revised Annex 1 has introduced significant changes affecting sterile medicinal product manufacturing, with an emphasis on contamination control, risk management and enhanced control on aseptic processes. As regulatory expectations evolve, pharmaceutical manufacturers must adapt to ensure compliance while maintaining operational efficiency.

Join our panel of experts to explore the key updates to EU GMP Annex 1 and their practical implications for sterile manufacturing. This session will provide valuable information on best practices for aseptic processing, contamination control strategies and the latest regulatory expectations.

Agenda:

• Introduction
• Contamination Control Strategy
• Barrier Technologies
• Aseptic Process Simulation
• Q&A