Blog & News - Validify

Subscribe to our newsletter

Computer Software Validation (CSV): Complete Guide for FDA-Regulated Companies

Everything you need to know about Computer Software Validation (CSV) — requirements, process steps, documentation, and how to automate compliance for 21 CFR Part 11 and GxP environments.

Software Risk Management: FDA 21 CFR Part 11, ISO 14971 & ICH Q9 Compliance

Learn how to implement software risk management in pharma, biotech, and medical devices - covering ISO 14971, ICH Q9, and FDA expectations. Includes templates and automation tips.

Modernizing Compliance with a Risk-Based Validation Approach

Traditional validation no longer fits modern systems. Learn how Validify supports risk-based validation to improve compliance and CSV. Read more.

GxP Validation: How Automation Improves Software Quality & Compliance

Learn how GxP validation and automation work together to improve software quality, reduce human error, and meet FDA & EMA compliance requirements.

FDA Software Risk Management: A Practical Guide for GxP Teams

FDA software risk management doesn't have to mean endless spreadsheets. Learn how to build a 21 CFR Part 11-compliant risk management process with real examples and a free template.

CSV Automation Software for FDA-Regulated Companies

CSV Automation can save time and reduce costs. Discover how it works and its benefits. Click to learn more!

Using Automation in Validation

Discover how automation enhances validation of cloud-based quality systems, ensuring compliance and efficiency with Validify’s expert solutions.

Computer System Validation has changed!

Discover the evolution of Computer System Validation and how Validify helps you stay compliant with the latest automated validation solutions.

From CSV to CSA: Understanding the Shift to Computer System Assurance

The FDA's shift from Computer System Validation (CSV) to Computer System Assurance (CSA) changes how you document and test software. Here's what it means for your compliance program.

FDA Computer System Validation Guidance: A Practical Guide in the Era of Automation & Cloud Platforms

FDA Computer System Validation Guidance for cloud & SaaS systems. Learn risk-based CSV strategies and modern compliance practices. Read more.

Modernize risk management in software validation

As SaaS becomes increasingly popular and companies are relying more and more on SaaS platforms, managing risk has become essential.

Moving to cloud based applications

Explore the benefits of moving to cloud-based applications and how Validify ensures smooth transitions with automated validation for compliance.

CSA new guidance release

Explore the new CSA guidance and how Validify helps streamline compliance with automated validation processes for software and systems.

The Risks in SaaS Based Applications

Uncover hidden risks in SaaS-based applications and learn how Validify mitigates them through automated validation and compliance solutions.

From CSV to CSA

Understand the transition from CSV to CSA and how Validify simplifies compliance with advanced automated solutions for software validation.

Salesforce Computer System Validation | Salesforce CSV

Discover the essentials of Salesforce Computer System Validation—why it’s crucial, how to leverage automation, and the right way to do it.

Our Blog