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Two Day Course: Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers (September 16-17, 2021)
Laura Wood of Research and Markets provides training on “Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers.” This course will educate you about various key elements of sterility assurance and contamination control such as Cleanroom Regulations, Classification, Sources and types of particles, Design Requirements, Validation/Qualification, Operations, Environmental Monitoring Program requirements, Excursion investigations, DataTrending, Microbiological processes/methodology, Cleanroom cleaning/disinfection. The types of micro-organisms, typical mitigation steps in ensuring an effective contamination control through Personnel Training (Aseptic Practices, Cleanroom Behavior and Contamination Control Procedures),Gowning Controls, Personnel Training, Cleanroom Trafficking (Cleanroom Personnel Material, Product and Equipment Transfer Practices and Training…
Published in Informational
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