Inside The Barrier: Optimizing Aseptic Processing With Isolator Technology

Sterility assurance is the bedrock of patient safety, and pharmaceutical isolators are the gold standard for maintaining the ultra-clean, contained environment required for aseptic processing and hazardous compounding. They are essential tools for manufacturers looking to meet the highest standards of cleanliness and containment.

This deep dive takes you inside the world of isolator technology, exploring the core design principles and engineering that enhance both operational efficiency and regulatory compliance. You’ll learn how these systems integrate with broader facility designs, including modular and mobile platforms, offering both flexibility and scalability for large-scale and niche drug manufacturing needs.

We’ll walk through real-world use cases and show how to effectively plan your validation pathway—from user requirement specifications (URS) to FAT/SAT, IQ/OQ/PQ, and airflow visualization. Furthermore, the session reviews how current regulations, like Annex 1 and ISO 14644, map to isolator design and essential documentation, including important VHP bio-decon cycle considerations.

Discover how to reliably scale your operations while ensuring maximum sterility and compliance. Access the full webinar to explore the future of aseptic manufacturing.