Join this insightful webinar, presented by Mariantonietta Brunengo, Business Developer at QSGroup, to explore the evolution of disinfectant selection for GMP Grade C and D cleanroom environments. The session challenges the traditional reliance on 70% IPA and examines how modern regulatory requirements, including EU GMP Annex 1:2022, Contamination Control Strategy (CCS) principles, sustainability objectives, operator safety, and total cost of ownership are reshaping decision-making processes. Participants will gain a practical understanding of risk-based disinfectant selection, comparing efficacy, material compatibility, HSE considerations, GMP compliance, and environmental impact to identify the most appropriate disinfection strategy for today’s pharmaceutical manufacturing facilities.
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