PDFeve® Bioprocess Platform Software
Software platform
eve® is able to do more than just plan, control and analyse your bioprocesses. The eve® software integrates workflows, devices, bioprocess information and big data in a web-based platform, with which you can organise your bioprocesses in a web based system.
Please click here to learn more about our software platform eve®.
Plan :
Plan up to 99 Batches simultaneously
Quickly plan batches with recipes
Plan and control batch strategies
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No programming needed
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Batch phase transition configurator
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Preconfigured functions
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Programmable functions without limitations for advanced
Control :
Compare running with completed batches
Soft-sensors (software-sensors)
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Easily create on your own
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Preconfigured INFORS HT soft-sensors
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Gain information from real time data
Save experiments as receipes
Automate batch completely or intervene manually
Simple comparison of batch processes
Knowledge:
Save all batch data in a central, fast NoSQL database (ElasticSearch)
Data and information management company-wide or work group-wide
Simple search, sorting, and filtering functions
5 libraries
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Experiments
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Organisms
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Culture media and media compounds
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Soft-sensors
Data import and export
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Data import formats: csv, excel, .eve, .iri
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Data export formats: .eve, csv
Connectivity :
Connect and manage any number of bioreactors and shakers, as well as analyzers*
Unlimited user access from everywhere without additional installation on clients*
Supported protocols: OPC XML DA, OPC DA, OPC UA, Modbus, analog and various proprietary protocols (ADI, DCU, various lab scale protocols, ...)
Monitoring and data visualization :
Monitoring of up to 80 batches*
Dynamic and fixed alarms for process parameter
Audit Trail
Data access via web interface from all computers in the network
Individually adjustable and storable charts
User Management :
6 predefined user roles:
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Manager
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Technician
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User
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Operator
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Guest
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System Administrator
Computer-IP-based access control for increased process protection
Automatic logoff and password renewal
Read-only access for guests and audits
Meets technical requirements for FDA 21 CFR Part 11 and EU GMP Annex 11 compliance
Reporting :
Comprehensive, customizable reports of planned, running and completed batches and experiments with all the recipe information
Export of reports at the touch of a button in e.g. PDF, Word, Excel and PowerPoint
Complete audit trail logs extensive information
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Batches, e.g. start batch, setpoints, offline sample, communication errors
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Setup environment, e.g. configuration, device
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User management, e.g. new user, log in/ou
Validation documentation :
For validating eve® in accordance with GMP requirements for computer-assisted processes.
eve® meets the technical requirements of FDA 21 CFR Part 11 and EudraLex Annex 11. INFORS HT offers two service packages
For a successful validation process, INFORS HT offers the following documentation:
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FDA declaration of conformity
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EMA declaration of conformity
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FS (Functional Specifications)
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IQ (Installation Qualification) protocol
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OQ (Operational Qualification) Test protocol
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