Many companies have spent an exorbitant amount of money and time on the qualification of cleanrooms and the validation of product manufactur
Many companies have spent an exorbitant amount of money and time on the qualification of cleanrooms and the validation of product manufactured within. KENX is proud to present a one-stop-shop for professionals tasked with the contamination control, cleanroom design and cleaning validation practices at their facility. This conference showcases those paving the way in best practices in cleaning validation, cleanroom qualification, disinfection, contamination control, environmental monitoring and more. This conference delivers more the 30 tutorials in:
Cleaning Validation & Critical Cleaning Processes
Implement a Risk-based Program
Set Acceptance Criteria and Health Limits
Determine Critical Process Parameters (CPP) and Critical Quality Attributes (CQA)
Implement a Continuous Monitoring Program
Cleanroom Validation and Qualification
Ensure state of control through airflow quality
Determine what tests need to be performed
Implement IQ/OQ/PQ Protocols
See the latest aseptic technologies and best practice
Contamination Control & Disinfection
Understand the regulations and develop a strategy
Design a process for effective residue removal
Identify contamination risks and conduct an assessment
Reduce validation timelines and cost
Environmental Monitoring
Determine types of sampling performed and implement
Trend data and analyze results
Understand the key components a summary report
Monitor viable and non-viable particles
Discussion
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