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CODE: TWENTY20
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Validity : 27th Apr'24 to 07th May'24
Cleanroom, Microbiology and Sterility Assurance Practices for Drug and Device Manufacturers
- 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.
Overview of the webinar
The types of micro-organisms, typical mitigation steps in ensuring an effective contamination control through Personnel Training (Aseptic Practices, Cleanroom Behavior, and Contamination Control Procedures), Gowning Controls, Personnel Training, Cleanroom Trafficking (Cleanroom Personnel Material, Product and Equipment Transfer Practices and Training (Entry and Exit Policy), Cleanroom Gowning, Contamination Control, Cleaning, and Disinfection Program and the Basics of Sterilization Processes- Physical and Chemical Processes will also be discussed.
The various regulatory bodies’ requirements such as 21 CFR Part 211 (mostly relevant 211.113 “Control of microbiological contamination”, ISO 14644 (Various Parts), FDA Guidance for Industry: Sterile Drug Products Produced By Aseptic Processing - Current Good Manufacturing Practice”) amongst others and the criticality of aseptic processing and other key contamination control evaluators during the manufacture and testing of products are important to the quality determination and release of the finished manufactured products.
Who should attend?
- QA Managers and Associates responsible for QC Oversight
- QC Analyst and Manager
- QA/QC/Compliance/Regulatory affairs professionals
Why should you attend?
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, Microbiological processes/methodology, Cleanroom cleaning/disinfection.
Faculty - Ms.Kelly Thomas
Ms. Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation; including, process/product validation, facilities validation, 21 CFR Part 11, test method validation, equipment/automated processes and cleaning validation.