Determining the efficacy of biocides is critical for maintaining the bioburden levels under control to have a safe, robust, reproducible pharmaceutical process.

However, qualification for biocides is challenging, requiring you to consider many parameters and regulatory requirements. Not doing it correctly may lead to contamination and regulatory complications, which could lead to the shutting down of business.

This training will help you consider the essential steps in biocide qualification on the surface and accomplish the authorities’ expectations.

It will ease the work of the operators and SMEs to understand how the biocide will maintain the bioburden of the facility under control.

Speaker
EU QA Associate / Consultant of pharmaceutical contamination control strategy

Marc García Gómez

Marc is an expert on the qualification of disinfectants and sporicides and validation of cleaning and disinfection processes of Pharmaceutical Facilities. Marc is the author of various articles in Spanish pharmaceutical magazines about cleaning and disinfection. Marc has performed training sessions in dozens of pharmaceutical manufacturing sites about personnel behavior, hygiene and gowning, cleaning and disinfection of surfaces, and Contamination Control Strategy, and Risk Analysis following ICHQ9 principles.

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