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PMX-MES report adjustment and creation
Project duration: 3 months
Brief description
The standard PMX-MES (Manufacturing Execution System) software is individually adjusted in accordance with the pharmaceutical company's requirements in order to fulfill certain guidelines (FDA, GMP) and to provide documentation in the form of reports.
Supplement
The List&Label tool is used for reporting in the PMX system. The layout of this report is customized. The data content and structure of the report is provided via a Python file. Data queries take place via integrated SQL queries from the Oracle database.
Subject description
Production departments in the pharmaceutical industry have to fulfill certain guidelines (e.g. GxP, FDA) and prove compliance in the form of reports.
Overview
- Industries pharmaceutical industry
- Specialist tasks FDA validation, GxP/GMP, Reporting
- DV tasks standard software support
- System environment Client/Server, standard software: industry systems
- Databases Oracle Database
- Development/ test tools Hora, UltraEdit,
- Standard software PMX-MES
Project period12.07.2004 - 22.10.2004
Contact
PTA GmbH Head Office
Weberstraße 2-4
D-68165 Mannheim
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