Does anyone know the steps necessary in rework of finished product? Can anyone spare a Rework procedure?Or a few indications?Thanks.
It will be more useful to know the genre of the product as well as its applications. That will be the minimal information required by the groups keen enough to help you for your query.
probably this link will be useful for you as it give sthe SOP fo rework procedurehttp://www.gmpqualityup.com/sample/QMS-065_sample.pdf
Sorry. I forgot to specify the domain. The rework procedure I am looking for is for pharmaceutical finished products (hidrosoluble medicinal powder) for veterinary use. On gmpqualityup site I have found a procedure (a part of it) that doesn't fit to our company. It is too restrictive. I could use some of your experiences if they are related to my domain. Thanks again.
by any chance you have an access code to GMPqualityup.com?
Sorry, I don't.