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Pharmaceutical production MES system replacement

Project duration: 1 year, 8 months

Brief description

Preparation and documentation for a complex system replacement of the MES individual software with the PMX standard software.

Supplement

It is important to ensure that the documentation fulfills the regulatory requirements of the authorizing bodies (FDA, EU). Furthermore, in-depth knowledge of the production processes and the previous software form a basis for precisely adjusting the future standard software.

Overview

Project period01.02.2003 - 30.09.2004

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Ole Knudsen

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