OOS and Cleaning Validation

Discussions about methods, troubleshooting and best practices across both pharmaceutical and biopharmaceutical analysis.

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Hello everybody. Are there guidelines for the management of the OOS during the Cleaning Validation phases?
I don’t know how to handle them. Whether as a laboratory OOS or process deviations.

Thanks!
I use 3M method (man-material-machine) or an extended fishbone analysis :)
2 posts Page 1 of 1

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