What exactly do you mean by validating LabVIEW in a cGMP production environment. Since LabVIEW is a development environment, I would assume that the specific software built in LabVIEW would need to be validated for use within the cGMP environment. Are you asking specifically for LabVIEW, or other NI products as well? Is this part of a system, or a stand-alone piece of software/device?
CLA, CLED, CTD, CPI
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