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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.
Latest News
Why Manual QbD Leads to Delays, Errors, and Ongoing Frustrations
Aug 28, 2025 10:15:00 AM | Manual QbD in pharma creates delays, errors, and frustrations. Discover how digital QbD frameworks enhance efficiency, accuracy, and compliance in drug development.
Posts about Chemistry, Manufacturing and Control (CMC):
Why Manual QbD Leads to Delays, Errors, and Ongoing Frustrations
Manual QbD in pharma creates delays, errors, and frustrations. Discover how digital QbD frameworks enhance efficiency, accuracy, and compliance in drug development.
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How Inefficiencies in Tech Transfer Drive Up Costs (And What to Do About It)
Discover how inefficiencies in tech transfer in pharma increase costs and delays—and how digital tools help reduce both cost and risk.
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How Spreadsheet Chaos Derails Quality by Design in Pharma
Learn how spreadsheet chaos undermines Quality by Design in pharma—and how digital QbD platforms support CMC manufacturing and development.
How to Apply a Quality by Design Framework with ValGenesis iCMC
Learn how ValGenesis iCMC integrates Quality by Design principles with CMC lifecycle management to enhance pharmaceutical process development.
All Tags
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
Quality Risk Management
Risk and Data as Knowledge Enablers: a Lifecycle Approach - ValGenesis
Read the industry insight on the topic of Quality Risk Management
Presented by
Sandra Silva
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.
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What Are the Regulatory Expectations for Cleaning Validation?
Learn why cleaning validation is important, what FDA and global guidelines require, and how a digital system can reduce risk and ensure GMP compliance.
Previously
Why Modernizing Cleaning Validation Is Crucial for Compliance
Why Established Pharma Sites Need a Digital Cleaning Validation Strategy
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.
Catalent's Journey of Continuous Improvement for CSV Excellence
Learn how Catalent scaled CSV compliance with ValGenesis VLMS to enhance global IT operations.
Previously
Validating Pharma 4.0 for Smart Manufacturing
The X Factor for Successful Digital Transformation in BioPharma: People
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