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2021 - Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers
Date2021-02-03 - 2021-02-04
Deadline2021-01-24
VenueVirtual Seminar, USA - United States 
KeywordsCleanroom regulations; Cleanroom classifications; Cleanroom qualification
Topics/Call fo Papers
Cleanroom Regulations, Classifications, Basic Background and Design Considerations
Cleanroom Qualification, Cleaning Validation (IOQ/PQ), Routine Monitoring and Excursion Investigation
Environmental Monitoring Program (Monitoring, Excursion Investigation and Trending of Data)
Personnel Training (Aseptic Practices, Cleanroom Behavior and Contamination Control Procedures)
Cleanroom Trafficking (Cleanroom Personnel Material, Product and Equipment Transfer Practices and Training (Entry and Exit Policy)
Cleanroom Gowning, Contamination Control, Cleaning and Disinfection Program
Basics of Sterilization Processes- Physical and Chemical Processes
Cleanroom Qualification, Cleaning Validation (IOQ/PQ), Routine Monitoring and Excursion Investigation
Environmental Monitoring Program (Monitoring, Excursion Investigation and Trending of Data)
Personnel Training (Aseptic Practices, Cleanroom Behavior and Contamination Control Procedures)
Cleanroom Trafficking (Cleanroom Personnel Material, Product and Equipment Transfer Practices and Training (Entry and Exit Policy)
Cleanroom Gowning, Contamination Control, Cleaning and Disinfection Program
Basics of Sterilization Processes- Physical and Chemical Processes
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Last modified: 2020-12-18 19:50:08