Reduce release cycle time, while improving the accuracy and consistency of your batch records.
To ensure conformance to regulatory requirements, pharmaceutical manufacturers must document manual and automated procedures throughout the production process. Managing these activities is time-consuming, error-prone, and often extends release time.
With DeltaV MES Electronic Batch Record Management, you can dramatically reduce production time cycles, while improving the quality of the batch and the accuracy of the batch record.
Gain real-time visibility for production orders with an integrated business and manufacturing system environment. DeltaV MES will automatically collect data to ensure data integrity, while embedded electronic workflows ensure process consistency.
Identify and resolve deviations that can impact product quality. Flag exceptions or deviations and use them to drive your quality review. Then focus on remediation steps to significantly reduce review time.
Build a fully integrated manufacturing execution system and distributed control system to create a single recipe execution environment. A fully integrated recipe streamlines testing, reduces system interface maintenance, and lowers total cost of ownership.
Materials Management
Ensure materials are dispensed correctly and accurately traced through the entire batch process
Quality Review Manager
Identify and resolve process exceptions early to reduce batch release time and ensure quality.
Equipment Management
Ensure operators and technicans have a complete understanding of the status of all equipment.
Information Integration
Integrate plant floor data with business systems to coordinate functions like process control, ERP, LIMS, and CMMS.
