Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers will educate you about various key elements of sterility .. Read more 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.
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