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an index of the qualification protocols code figures linked to the different instruments that happen to be used in the preparation process, together with the similar qualification dates, While using the aim to exhibit that the above mentioned devices position is compliant with the general validation plan;Realize a controlled state of validation wit
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??????????????????????????????????????????????????????????????????????Create a doc retention plan that defines retention durations for every doc form dependant on authorized and compliance requirements. Put into practice safe deletion practices aligned with regulatory needs.Mainly because a customer and vendor need to be concerned it should not iss