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Totally Integrated Batch
DeltaV Batch is easy with a completely integrated database that coordinates all configuration activities; system information is transparently distributed globally in the run-time environment so each part knows about the others.
Engineering The Batch engineering environment is based on the ISA S88.01 standards for equipment, procedural and state transition models. Utilizing standards-based software minimizes training and maintenance costs.
Execution DeltaV Batch has controller-based phase logic closely coupled with the batch executive that executes recipes - no mapping data with third-party products - it's all seamlessly integrated!
Production Scheduling Campaign Manager is a fully integrated component within the DeltaV Batch software. Campaign Manager helps you easily define and create campaigns. Solutions are also available for enterprise-based campaign scheduling.
Production Information Management The DeltaV Batch Historian is also fully integrated within DeltaV Batch. No configuration is required to collect batch data, and this data is graphically represented based on the S88 models in the Batch History View. For complete plant-wide information management our industry experts can help you design and implement DeltaV Batch with the DMI Compliance Suite. This solution provides one complete batch record for both your automated and manual procedures.
Compliance Support
DeltaV Batch makes it easy to comply with FDA and other government regulations.
21 CFR Part 11 DeltaV Version Control and Audit Trail (VCAT), Recipe Authorization, Operator Actions with Confirm/Verify, Batch Historian and Electronic Operator Log help you meet 21 CFR Part 11 compliance more easily than other non-integrated approaches. DeltaV Batch and the DMI Compliance Suite help you maintain documentation for both automated and manual procedures in one place. For more, read our whitepaper on DeltaV Capabilities for Electronic Records Management.
PAT – Process Analytical Technologies In September 2004, the FDA issued a "Guidance for Industry" called PAT – A Framework for Innovative Pharmaceutical Manufacturing and Quality Assurance for the Pharmaceutical industry. Although named Process Analytical Technologies, one shouldn’t take the term ‘analytical’ too literally. The focus of the PAT guidance is for better understanding of the process which in turn leads to better quality products for the consumer and lower costs for manufacturers.
Process understanding can happen in many different ways. The draft guidance lists four groups of tools that can implemented for PAT:
- Multivariate data acquisition and analysis tools
- Modern process analyzers or process analytical chemistry tools
- Process and endpoint monitoring and control tools
- Continuous improvement and knowledge management tools.
Emerson Process Management has the tools and industry expertise to help you design and implement the PAT framework to improve your operation's performance with embedded neural network technology for measuring real-time quality. For more, read "Getting Important Quality Measurements in Real-Time" or contact our Life Science experts for assistance.
DeltaV Batch makes it easy.
Check out the results of companies already benefiting from DeltaV batch, see it for yourself in action, learn more from the Product Data Sheets and Whitepapers, and find more information specific to your industry needs.
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