The FDA perspectives on cleaning validation and areas of concern during regulatory inspections
The importance and underlying principles of cleaning validation and the requirements to have adequate cleaning procedures for manufacturing equipment in contact with the product
How to prepare and defend your own cleaning validation approach/program and avoid costly delays and/or rejections by regulatory agencies
Cleaning validation procedures, protocols and reports that meet current FDA, WHO, PIC/S and EU regulations
Who should Attend
Quality professionals
Senior quality managers
Validation engineers
Production supervisors
Quality engineers
Process owners
Quality auditors
Past Events
Regulatory Requirements and Principles for Cleaning Validation 2016 - 08-09 Sep 2016, San Francisco, California, United States (58363)
Regulatory Requirements and Principles for Cleaning Validation 2026
Important
Please, check "Regulatory Requirements and Principles for Cleaning Validation" official website for possible changes, before making any traveling arrangements
