The Benefits of Automating Your Requirements Traceability Matrix
Automate your requirements traceability matrix to improve efficiency, reduce compliance risks, and streamline validation for better audit readiness.
Latest News
What is a Multi-Site Digital CPV, and Why Should You Want It?
Oct 25, 2024 4:32:28 PM | A Multi-Site Digital CPV system allows you to manage and monitor manufacturing processes across multiple sites in real-time.
Posts about Digital CPV:
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 CPV optimizes pharmaceutical manufacturing, reducing time, costs, and errors through real-time monitoring and automated processes.
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?
In this blog post you'll know the differences between Manual CPV vs Digital CPV and how we can help you on its implementation.
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".
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
Catalent's Journey of Continuous Improvement for CSV Excellence
Are You Aligned with FDA's Computer Software Assurance Methodology?
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.
Why Established Pharma Sites Need a Digital Cleaning Validation Strategy
Discover how digital cleaning validation strategies can modernize established pharma facilities, ensuring compliance, efficiency, and patient safety.
Previously
Is Your Cleaning Validation Stuck in the Slow Lane?
Cleaning Validation Program Compliance: Build a Framework for Success
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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