Cleaning process validation
Learn how to prevent cross-contamination and develop cleaning strategies under GMP, FDA, and WHO guidelines.
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Is your company prepared to face regulatory inspections focused on cleaning processes?
Many regulatory observations arise due to:
- Poorly defined cleaning procedures
- Incorrect acceptance limits
- Non-representative sampling
- Lack of worst-case analysis
- Inadequate analytical methods
- Failure to maintain the validated state
What Will You Learn?
- TOPIC 1
Fundamentals of pharmaceutical cleaning
- TOPIC 2
Types of cleaning processes
- TOPIC 3
Worst-case selection
- TOPIC 4
Determination of acceptance limits
- TOPIC 5
Analytical validation
- TOPIC 6
Sampling techniques
IMPORTANT: All sessions are LIVE and WILL NOT BE RECORDED. We recommend scheduling these dates in advance so you don’t miss them.
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