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About the Workshop
Cleaning Validation plays a crucial role to verify the effectiveness of cleaning procedures and ensure no risks are associated with cross contamination which harms the patient safety. The primary objective of this workshop is to ensure that pharma companies are able to successfully pass their FDA inspections by following the effective cleaning validation techniques. This workshop will discuss about Cleaning Validation guidelines, practices and innovations that include development of cleaning process programs and cleaning verification and validation programs. The Workshop Trainer will discuss regulatory validation guidelines and show how quality risk management should be utilized in implementation of risk-based lifecycle approach to cleaning validation.

During this 2-day workshop, the trainer will also touch upon use of statistics in the process of cleaning validation and talk about continued verification/monitoring. The focus would be on a risk-based approach as it is a corner stone of cleaning process validation principals and practice. This will be an interactive workshop.

For registrations, please submit the following information: