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Automate your requirements traceability matrix to improve efficiency, reduce compliance risks, and streamline validation for better audit readiness.

Learn how Catalent scaled CSV compliance with ValGenesis VLMS to enhance global IT operations.

If you’re following these 3 core principles, odds are you’re already aligned with the FDA's computer software assurance (CSA) methodology.

Learn how to reduce costs, improve accuracy, and enhance compliance by integrating vendor-provided testing into your validation framework.

Learn how traditional CSV conflicts with Agile development principles and why computer software assurance (CSA) is a better fit for Agile environments.

Unlocking the potential of Computer System Assurance (CSA) in pharmaceuticals: A roadmap for a seamless transition from CSV to CSA.

How do we deliver objective evidence with a high degree of certainty it will withstand regulatory scrutiny? Technology tools like a VLMS hold the answer.

In this blog post, we will explore how making your transition from the traditional CSV to the new CSA approach can save you time and resources.

Writing good requirements during the requirements management process is the key to better product quality, accelerated development, and less rework.

A better resource use, a simpler process, and a superior product quality. These are some of the CSA benefits explored in this blog post.