Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers
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Topic : Health and Medicine; Pharmacology and Drug Development
Engineering and Technology; Keywords: Design
Description :
Topics: Cleanroom regulations, Cleanroom classifications, Cleanroom design considerations, Cleanroom qualification, Cleanroom cleaning validation IOQ/PQ, Cleanroom Routine Monitoring and Excursion Investigation, Cleanroom Environmental Monitoring Program, Environmental Monitoring Program, Cleanroom Monitoring, Excursion Investigation and Trending of Data, Cleanroom Personnel Training, Aseptic Practices, Cleanroom Behavior and Contamination Control Procedures, Cleanroom Trafficking, Cleanroom Gowning, Contamination Control, Cleaning and Disinfection Program, Sterilization Processes- Physical and Chemical Processes, basic concept of microbiology, microbiological and contamination control practices
Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers to be held in Dallas, TX, United States between 25 May 2020 and 26 May 2020. It is organised by Complianceonline. It covers specific areas of Health and Medicine such as Pharmacology and Drug Development. Visit the website of the conference for more detailed information or contact the organizer for specific questions.
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