ValGenesis Product Suite and Integration Support
Your ValGenesis Partner
Westbourne is an approved ValGenesis Partner. With our extensive expertise in the pharmaceutical industry, we offer comprehensive ValGenesis support. You will benefit from our extensive experience working in pharmaceutical laboratory and manufacturing environments, providing best-in-class technology support (IT and OT – operational technology) with a robust scientific underpinning.
Our team can help throughout your entire ValGenesis journey, from selecting the right product for your needs to implementation planning, system integration, platform configuration, user training, and ongoing support.
ValGenesis Product Range
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Validation Lifecycle Suite
iVAL
iVal fully supports CSV, CSA, and CQV methodologies. It enables centralised planning with key features that include AI-powered test authoring, automated test execution, live anomaly flags in real-time, full traceability, and enhanced oversight.
iClean
iClean is a digital cleaning validation platform that halves cleaning times and automates calculations to eliminate errors. It enables full standardisation of cleaning strategies while delivering real-time, intelligent, and automated oversight.
Rule-driven workflows, 2D and 3D equipment maps, and automated MACO calculations are among the range of features that reduce manual cleaning validation processes. They also eliminate human error, ensure consistency, and streamline compliance.
iOps
iOps is a digitalised operation execution platform for routine activities such as equipment use, maintenance, cleaning, quality checks, and calibration. It replaces error-prone, inconsistent, and incomplete paper logbooks to ensure consistent and reliable real-time capture of critical activities.
iOps enhances visibility and control with timestamped audit trails while automating reviews, alerts, and deviations for enhanced compliance. It provides complete traceability and significantly reduces manual processes.
Process Lifecycle Suite
iCMC
With iCMC, you can digitalise and centralise process and analytical development with a scientific underpinning and digital QbD framework that is suitable for all CMC stages. It helps you ensure consistency and meet compliance requirements, while reducing manual effort.
Apply risk assessment tools that are industry-standard for common pharmaceutical processes, including PHA, FMEA, and HAZOP. There is also full support out of the box for CQA and CPP analysis, as well as QTPP definition.
iCPV
iCPV enables real-time monitoring and automated data analysis to digitally transform and centralise continued process verification. With intelligent analytics, guided workflows, early warning insights, and automated reports, iCPV ensures consistent quality across all product batches.
With iCPV, you can monitor critical process parameters and critical quality attributes, improve decision-making, and confidently design and manage continued process verification programmes.
Westbourne Expertise
Westbourne has unique experience and expertise to help you make the right decision and maximise your ValGenesis investment. We have extensive experience delivering IT, operational technology, validation, and support solutions to clients in the pharmaceutical industry. We have skilled technical and scientific resources on our team, and we are approved ValGenesis partners.
Our experts will support you every step of the way, from deciding on the platform you want to use to planning, implementing, and configuring ValGenesis in your facility. We will also fully integrate the platform with your existing systems, and we can provide comprehensive training and ongoing support to maximise adoption, build user confidence, and ensure continuous improvement.
ValGenesis FAQs
How does ValGenesis support regulatory compliance in the pharmaceutical industry?
ValGenesis is built with compliance at its core. The suite of products provides electronic records and signatures that are 21 CFR Part 11 and EU Annex 11 compliant, as well as full audit trail functionality and validation-ready configurations. By digitalising and automating validation, quality, and risk management processes, you can reduce manual errors, maximise data integrity, and ensure real-time traceability.
What ROI can we expect from implementing ValGenesis compared to traditional paper-based validation?
With expert support from Westbourne and the industry-leading ValGenesis platform, you can expect to see significant ROI through time savings, cost reductions, error reductions, and faster product launches. For example, the ValGenesis software suite lets you automate workflows to eliminate manual processes and redundant documentation. This can reduce validation cycle times by up to 50%. And by centralising data, you can minimise compliance risks and costly regulatory breaches.
Can ValGenesis integrate with our existing systems (ERP, MES, LIMS, QMS)?
Yes, the ValGenesis suite of products offers seamless integration capabilities with leading ERP, MES, LIMS, QMS, and other enterprise platforms. At Westbourne, we provide the technical expertise to ensure the successful integration of ValGenesis products across your technology stack. This ensures smooth data flows while eliminating data silos and entry duplication.
Pharmaceutical Digital Transformation
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Pharma Lab and Manufacturing
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On-Site ICT
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Validation
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Global Service Desk
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