Opcenter Execution Pharma expedites required design, execution and review steps to ensure fully compliant, fully documented pharmaceutical production.
Use master batch record (MBR) driven manufacturing
Ensure that every detail of your production operation is recorded with our master batch record-driven approach. Our MES for pharmaceuticals supports thorough planning of your documentation process, including product definition, resource requirements, process definitions, quality management plans and batch review and release procedures. The MBR incorporates values directly from the automated recipe.
Streamline fully compliant manufacturing execution
Optimize batch manufacturing processes that are fully compliant with the U.S. Food and Drug Administration (FDA) and good manufacturing practice (GMP) regulations. Opcenter Execution Pharma helps you to streamline resource availability, such as user guidance, equipment allocation and standard operating procedures. It systematically controls execution at all stages, either human operations or operations controlled by the automation layer.
Leverage paperless batch record management
Simplify batch record management by providing a single point of storage and access to all batch-related documents. Paperless management by our MES for pharmaceuticals reduces the time and effort spent on batch records preparation, maintenance, review and release, and it minimizes the time needed to access information from the MBR. The system facilitates a review of the batch record by exception, resulting in faster and more efficient product releases.
Enjoy true paperless manufacturing
Use a single interface to manage all regulated processes without paper-based procedures and documents. Opcenter Execution Pharma enables native integration with the production control system, reducing complexity and making configurations easier. It also provides easier and more efficient navigation for the operational staff, as well as a centralized point of review for alarms, events and reports.
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