Cleaning validation for product dedicated chromatography columns, tanks and bioreactors

["Arvind Kushwaha" <Arvind.Kushwaha@intasbiopharma.co.in> (by way ofJohn Dolman <info@the-dolman-consultancy.com>)]

Dear Forum,

     What is general industry practice for cleaning validation for
product dedicated chromatography columns, tanks and bioreactors? Being
product dedicated, there is no risk of product carryover to another
product, so how are limit of acceptance calculated for cleaning
validation?

Thanks in advance,
Arvind
  

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