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2020 - Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers
Date2020-07-22 - 2020-07-23
Deadline2020-07-12
VenueVirtual Seminar, USA - United States 
KeywordsCleanroom regulations; Cleanroom classifications; Cleanroom qualification
Topics/Call fo Papers
Discuss Cleanroom Classification, Regulations and Guidelines
Summarize how to Perform Cleanroom Design, Validation/Qualification, Operation, Environmental Monitoring Program and ensuring a state of control
Describe Aseptic Practices, Personnel Health Practices, Gowning and Trafficking Patterns in a Cleanroom
Establish and describe the Requirements of Cleanroom Cleaning/Disinfection and Contamination Control Practices
Summarize various Sterilization Processes, Advantages and Disadvantages –both Physical and Chemical
Describe the Sterilization Processes and Controls
Summarize how to Perform Cleanroom Design, Validation/Qualification, Operation, Environmental Monitoring Program and ensuring a state of control
Describe Aseptic Practices, Personnel Health Practices, Gowning and Trafficking Patterns in a Cleanroom
Establish and describe the Requirements of Cleanroom Cleaning/Disinfection and Contamination Control Practices
Summarize various Sterilization Processes, Advantages and Disadvantages –both Physical and Chemical
Describe the Sterilization Processes and Controls
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Last modified: 2020-06-24 22:19:57