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Validation support for SAP implementation
Project duration: 11 months
Brief description
In the course of implementing the SAP standard software in a validated environment (GMP), a medical product manufacturer's business processes are harmonized with the business processes at an affiliate. Test management and test plan creation are based on a comprehensive risk analysis of the logistical areas: production, storage and materials management.
Subject description
Business knowledge and experience of the MM, PP and Warehouse Management SAP modules forms the basis for creating test plans in the logistical area (production, storage, materials management). This knowledge and experience makes it possible to supervise the tests professionally. The chemical-pharmaceutical sector and the company's position within an international group pose particular challenges to the implementation of the SAP standard software (FDA compliance, GMP).
Overview
- Industries health care
- Specialist tasks FDA validation, GxP/GMP, logistics, test coordination, test management, validation
- DV tasks standard software launch
- System environment standard software: ERP systems
- Procedure model customer standard
- Standard software SAP R/3 LE, SAP R/3 MM, SAP R/3 PP, SAP R/3 WM
Project period01.03.2008 - 31.01.2009
Contact
PTA GmbH Head Office
Weberstraße 2-4
D-68165 Mannheim
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