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
Retrospective vs. Automated CPV: Why Traditional Approaches Fall Short
Mar 12, 2026 9:00:02 AM | Move beyond retrospective CPV. Learn how automated CPV creates a continuous feedback loop to spot variability earlier and keep processes in control.
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Retrospective vs. Automated CPV: Why Traditional Approaches Fall Short
Move beyond retrospective CPV. Learn how automated CPV creates a continuous feedback loop to spot variability earlier and keep processes in control.
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.
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.
Avoiding the Pitfalls of PQRs with Digital Solutions
Learn to enhance Product Quality Reviews (PQRs) with digital solutions that drive quality improvement and regulatory compliance in pharma manufacturing.
Optimizing Your Annual Product Quality Reviews (APQRs)
Explore how digital transformation in pharma manufacturing enables continuous process verification and data-driven quality insights for better APQRs.
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.
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.
4 Life Sciences Lessons from the PAT to QbD Journey
In our journey to instill quality culture across life sciences, we've learned several valuable lessons along the way. The bottom line: continued training and development matters more than ever.
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.
Process Analytical Technology in Continuous Manufacturing
Learn how Process Analytical Technology (PAT) enhances continuous manufacturing in pharma, improving process control, product quality, and operational efficiency.
Cell and Gene Therapy: the Benefits of PAT and QbD
Cell and Gene Therapy products are considered the future of medicine. PAT and QbD can bring many benefits to C>
Digital 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.
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Featured Content
Quality Risk Management
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
Tech Transfer & Process Scale-up
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.
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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.
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Change Impact Assessments in ValGenesis iClean™: A Framework for Consistency
Discover how ValGenesis iClean™ standardizes change impact assessments in cleaning validation, enhancing consistency and compliance across teams and sites.
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Unlocking Operational Capacity with Fully Digitalized Cleaning Validation
The Real Cost of Bottlenecks: Why Manual Cleaning Validation Increases Regulatory Risks
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