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2021 - Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers
Date2021-09-16 - 2021-09-17
Deadline2021-09-06
Venue, 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
Other CFPs
- PV (Pharmacovigilance) Audit Strategy Planning - A Practical Approach to Design and Implementation
- Navigating through Maze of In-vitro Diagnostics (IVD) Regulations: A systematic approach from Regulatory Strategy to Regulatory Approvals in U.S./Europe/Canada
- Change Control Best Practices - Avoiding Unintended Consequences of Changes
- Technical Writing for Pharma, Biotech and Medical Devices
- Regulatory Compliance for Dietary Supplements in the US, EU and Canada
Last modified: 2021-07-17 18:56:53