Transitioning from CSV to CSA: A Practical Roadmap for Pharma Companies
For decades, the pharmaceutical industry has been bogged down by the heavy documentation burden of Computerized System Validation (CSV). If you work in quality assurance or IT validation, you know the pain: spending more time taking screenshots and writing extensive scripts than actually testing the software’s quality. The good news is that the tide is […]
CSV vs CSA in 2025: What Changes and What Doesn’t
Computer software assurance is the FDA’s risk-based way to build confidence in software that supports production and quality activities. If you have lived in classic CSV world, this post explains CSA vs CSV, where CSA applies, what stays the same, and how to roll it out in 90 days. We also cover FDA CSA guidance, […]
Challenges in Maintaining Data Integrity and How to Overcome Them
Challenges in maintaining data integrity is important for reliable decision making. When you can maintain data integrity, every report, every analysis, and every operation rests on solid ground. Yet even small teams face data integrity issues that can slow projects, erode trust, and drive up costs. In this blog, we’ll explore: As Validfor, a digital […]
