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ValConnect Innovation Day Princeton: A Glimpse into the Digital Future of Life Sciences
ValConnect Innovation Day Princeton brought Bayer, GSK, Cardinal Health, Transcat & Hansa Biopharma together to explore AI & Smart GxP™ in life sciences.
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Latest News
Prevention Over Reaction: Why Modern CPV Requires Automated Process Monitoring
Jan 8, 2026 9:30:01 AM | Discover how automated process monitoring in CPV ensures continuous control, early risk detection, and improved quality oversight in modern manufacturing.
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Prevention Over Reaction: Why Modern CPV Requires Automated Process Monitoring
Discover how automated process monitoring in CPV ensures continuous control, early risk detection, and improved quality oversight in modern manufacturing.
Digital Cleaning Validation: From Lifecycle Control to Real-Time Assurance
Discover how digital cleaning validation software like ValGenesis iClean™ is enhancing compliance and operational efficiency in the pharma industry.
ValConnect Innovation Day Princeton: A Glimpse into the Digital Future of Life Sciences
ValConnect Innovation Day Princeton brought Bayer, GSK, Cardinal Health, Transcat & Hansa Biopharma together to explore AI & Smart GxP™ in life sciences.
What is a Multi-Site Digital CPV, and Why Should You Want It?
A Multi-Site Digital CPV system allows you to manage and monitor manufacturing processes across multiple sites in real-time.
Save Time and Resources with Digital Continued Process Verification
Discover how digital continued process verification (CPV) drives process optimization in pharmaceutical manufacturing, reducing time, cost, and errors.
What Changes When Your CPV Goes Digital - A ValGenesis Story
Explore the essential role of CPV in your manufacturing process and discover the transformative impact of going digital in this blog post case study.
3 Huge Benefits of Integrating Process Data with Risk Management
In this post, we’ll look at 3 benefits of integrating process data with risk management and how it increases organizational efficiency and competitiveness.
Enhancing Continuous Manufacturing with Digital CPV Integration
Learn how implementing digital CPV plans can contribute to continuous processes reaping the benefits of Industry 4.0 and digitalization.
Manual CPV vs Digital CPV: Why Should You Upgrade?
Discover how digital CPV enables real-time quality monitoring in pharma and supports continued process validation across the product lifecycle.
How to Set up a Digital CPV Plan in 3 Steps
In this blog post, we'll give you some tips that help you setting up a Digital CPV plan in only three steps.
CPV Implementation: how to do it?
This blog post will give you a few tips on how to do a CPV implementation and the different requirements you need to make it successful.
How to Support Global Manufacturing of Pharma Products
Process, product performance and comparability are key to global production. This is how to support global manufacturing of pharma products.
ValConnect 2022 Session Round-up: CPV for New and Legacy Products
“CPV is a broader concept because it gives you a more holistic picture of overall product performance over a period of time. While both APR and CPV give you an indication of product performance, the current situation in most companies is that they remain disconnected".
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Featured Content
Root-Cause Analysis
Finding the Root Cause in mAB Production: a ValGenesis Story
Learn how we helped a customer find the root cause of a problem in monoclonal antibody (mAB) production and become stronger.
Written by
Sofia Santos
Process Digitalization
How to Accelerate Process Scale-Up With Effective Tech Transfer
There's a need to accelerate pharma product development and process scale-up. Having an effective tech transfer strategy can help you.
Written by
Sofia Santos
Cleaning Validation
Risk-Based Cleaning Validation: A Lifecycle Approach
Explore the evolution of pharmaceutical cleaning validation from compliance-focused practices to a risk-based, lifecycle-driven approach.
Written by
Kenneth Pierce
CSV and the Shift to CSA
CSA flips the paradigm of traditional CSV to "right-size" validation processes. Learn more about the benefits and principles of the CSA approach, which encourages critical thinking and automation.
Previously
The Benefits of Automating Your Requirements Traceability Matrix
Catalent's Journey of Continuous Improvement for CSV Excellence
Cleaning Validation
Learn how digitization offers a consistent way to carry out cleaning validation lifecycle activities, ensuring your methods and procedures are risk-based and rooted in scientific evidence.
Unlocking Operational Capacity with Fully Digitalized Cleaning Validation
Discover how fully digitalized cleaning validation boosts efficiency, ensures compliance, and transforms operational capacity in pharmaceutical manufacturing.
Previously
The Real Cost of Bottlenecks: Why Manual Cleaning Validation Increases Regulatory Risks
Digital Cleaning Validation: From Lifecycle Control to Real-Time Assurance
Pharma 4.0
Waves of new technology and thinking — IoT, AR, cloud, Agile — are transforming the very foundation of validation processes. Learn how to leverage them in a Pharma 4.0 world.
Unlocking Operational Capacity with Fully Digitalized Cleaning Validation
Discover how fully digitalized cleaning validation boosts efficiency, ensures compliance, and transforms operational capacity in pharmaceutical manufacturing.
Previously
Catalent's Journey of Continuous Improvement for CSV Excellence
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