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Elektronische Daten in der Arzneimittelherstellung: Vorteile der papierlosen Berichterstattung (Serie Teil 2 von 6)
In this six-part blog series, we examine common issues with data transfer, integrity, analysis, reporting and storage that we encounter as cleanroom owners and users every day. We’ll explore how automation and electronic solutions, within the parameters of Regulatory Authorities and cGMP, can help improve efficiency and product quality.
