Why Attend?
- Understand isolator types, regulations, and process risks impacting compliance and inspections.
- Learn from real-world case studies presented by industry experts, covering cycle development strategies and troubleshooting qualification challenges.
- Master open-door set-up through understanding of contamination risks and implementation of appropriate controls.
- Strengthen glove integrity management, including material selection, leak testing, sterilisation, and microbiological sampling.
Who Should Attend? Sterile manufacturing, QA, validation, microbiology, regulatory, and engineering professionals involved in aseptic processing.
