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Effective processes extending from material requirement planning to quality control
The adaptable SAP module Production Planning (PP) supports the entire production process. Fresenius Netcare implements this module Europe-wide and has also connected subsystems (weighing systems, production control terminals) of various suppliers in various locations. Our extensive know-how of the SAP standard allows us to extend the functionality in accordance with the customer's individual requirements without actually modifying the standard itself.
The PP module supports the following system processes:
- material requirements planning
- planned orders
- production order management
- capacity planning
- product cost accounting
- production information system/reporting
- connection of sub-systems, e.g. weighing systems and production control terminals
If you attach value not only to efficient production but also to secure and validated processes, we can provide you with the SAP module Quality Management (QM) which handles the planning, execution and monitoring of quality management processes. Fully integrated into the SAP system environment, detailed quality inspections can be planned and controlled in accordance with the statutory requirements. In addition, stability tests can be carried out using SAP QM and these are optimally supplemented in terms of planning, calculation and administration by the add-on stabilities from Fresenius Netcare.
To guarantee adherence to technical standards and ensure the high quality of your medical equipment, the SAP module Plant Maintenance (PM) provides a package that is integrated into other SAP functions for device, building and plant management. This package does, of course, comply with all of the applicable statutory requirements and provisions. This module also focuses on maintenance management within the framework of individually adaptable maintenance structures.
A further development from Fresenius Netcare paves the way for the system-supported management and maintenance of your medical equipment. This enhancement was developed in accordance with the statutory requirements arising from the Medical Devices Act and the Medical Devices Operator Ordinance.
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