Cleaning validation is increasingly important in preventing cross contamination and interactions between active ingredients in subsequent batches run in the same equipment. Emphasis will also be placed on interrelationships with other processes and using the information gained during validation to monitor and control the cleaning process to prevent failure.

Areas Covered in the Session:

• Sterilization process description and validation options including the kinetics of lethality (bioindicator vs bioburden) and test methods
• Pre-validation activities including defining worst case challenge to the process and selecting cleaning agents.
• Aspects to consider when writing the validation protocol.
• Sources of process variation and basics of process control
• Data collection and troubleshooting
• Post-validation (re-validation) and change control
• Reporting and documentation requirements

Who Will Benefit:

This webinar will benefit any organization that wants to validate and improve the effectiveness of their cleaning processes.  Those who will benefit include QA and Manufacturing Managers and Engineers who are responsible for validating cleaning or sterilization processes, Consultants, Auditors and responsible executives.