General description
Bio4C ProcessPad™ software is a data collection, visualization, and analytics platform that enables bioprocess monitoring, lifecycle management, reporting, investigations, and continued process verification (CPV).
Intelligently combining process data from disparate data sources generated during batch execution into a single, contextual, integrated data source, Bio4C ProcessPad™ software ensures process information is current, complete, and accessible throughout the product lifecycle.
If you are interested in learning more about the Bio4C ProcessPad™ software, please contact us today.
Services:
Intelligently combining process data from disparate data sources generated during batch execution into a single, contextual, integrated data source, Bio4C ProcessPad™ software ensures process information is current, complete, and accessible throughout the product lifecycle.
If you are interested in learning more about the Bio4C ProcessPad™ software, please contact us today.
Services:
- Installation/deployment services
- Validation package
- Validation services
- Software training
Features and Benefits
- Intuitive browser-based interface
- Automatically aggregate data from various sources into analysis-ready format
- At-a-glance process understanding with data visualizations
- Streamlined regulatory reporting with automated and templated reports
- Improve process robustness and reduce the risk of batch loss with real-time MVDA process monitoring tunnel
- Democratize data for global teams, CMOs, and suppliers with easy data, analytics, and visualizations sharing
- Automate and simplify CPV
- Designed to facilitate regulatory compliance and audit readiness
Legal Information
ProcessPad is a trademark of Merck KGaA, Darmstadt, Germany
Analysenzertifikate (COA)
Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.
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Artikel
Continuous process verification maintains drug product quality and regulatory compliance throughout production.
How software can simplify 21 CFR Part 11 and EudraLex Volume 4 Annex 11 compliance and provide additional benefits such as access control, audit trails and easier search and retrieval.