7 – 8 December 2026
TRAINING TIMES
Learn how VHP/vHâ‚‚Oâ‚‚ works, its bi-phasic process, and how to apply it effectively in contamination control, aligned with Annex 1 and ICH Q9(R1).
Handle BI quality issues, including “Rogue BIs,” with scientific approaches to ensure reliable cycle qualification.
Explore case studies covering isolators, RABS, cleanrooms, and biologics. Gain proven tactics for cycle optimization and material transfer.
Ensure VHP processes meet FDA, EMA, and MHRA expectations. Support inspections, avoid requalification issues, and maintain GMP compliance.
Three days of expert-led Zoom sessions packed with discussions, Q&As, and real-world scenarios.
All slides, tools, and supporting materials available in one place - before, during, and after the course.
Receive a digital certificate (also LinkedIn-ready) that verifies your skills in strategic trial planning.
Explore the fundamentals of vapour phase hydrogen peroxide, its bi-phasic action, and critical control points across the decontamination lifecycle.
Gain practical insight into regulatory frameworks like EU GMP Annex 1 and ICH Q9(R1), and how they apply to VHP process design and qualification.
Learn structured approaches for developing, qualifying, and requalifying VHP cycles using biological and chemical indicators and handling “Rogue BIs.
Understand how to investigate failures, identify root causes, and differentiate process issues from indicator quality problems.
Master application of VHP across isolators, RABS, cleanrooms, and material transfer systems, tailored to product types like biologics and ATMPs.
Designed for professionals who want to enhance their expertise and advance their careers
“I was really impressed by the trainer’s great knowledge and expertise.”Zeljko Joksimovic
“Mr. Drinkwater’s expertise on the subject was greatly appreciated.”Leonardo Ciofi
“Both the presentation and the Q&A session were very informative and valuable.”Kelvin GanMosi
