MIT systems are the connecting link between enterprise management and automation level. They are designed to support planning, control, optimization and quality assurance tasks in manufacturing processes.
In the field of the pharmaceutical industry, MIT systems cover virtually all subareas such as process development, clinical trial manufacture (CTM) and the production and packaging of a wide spectrum of products ranging from solid and liquid dosage forms, active ingredients, vaccines, diagnostic agents to technical medical components.
As an essential part of the overall IT strategy of pharmaceutical companies MIT systems have today become indispensable strategic instruments for production management and control. In interaction with enterprise resource planning (ERP) software for business process management and with automation systems (DCS, SCADA, PLC) MIT systems enable a holistic approach to the management of all production workflows.
Manufacturing Execution Systems (MES) are the essential central components of MIT systems. They constitute the core building block that integrates LIMS, Data Historian and other components neatly with one another and include all quality-relevant specifications and data.
The business functions provided by PAS-X as well as all associated services are specifically tailored to meet the requirements demanded by
Regulatory Compliance.
Business functions of independent but integrated MES systems, which ensure the optimum performance of the processes in the pharmaceutical industry, offer considerable technical advantages as compared to ERP or DCS add-ons and are also significantly cheaper to implement, validate and maintain.
Based on this insight we have developed PAS-X as a fully independent standard software package for the highly regulated and batch-oriented process industries. As a standard product, PAS-X provides out-of-the-box maximum standard functionality for applications in the pharmaceutical sector. PAS-X has not been designed as a tool set - on the contrary, it constitutes a qualified standard system, which is ready for validation and covers all essential business processes in the pharmaceutical industry.
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