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,…
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