Take Charge of Validation Debt in your Life Sciences Organization
Mounting validation debt is costing life sciences companies time and money. ✓ Learn how to recognize and resolve it ...
Automation: The Future of Paperless Validation in Life Sciences
What is paperless validation? Read our blog to learn about paperless validation software for life sciences and why it's ...
Building Risk Assurance into Life Sciences Computer Systems Validation with Automated Workflows
Deploy a risk assessment strategy to prioritize high vs. low tasks and stay current with system releases. ✓ Learn all ...
What is Computer System Validation?
What is computer system validation? Learn the importance of computer system validation with Sware. ✓ Discover how it ...
What is Process Validation?
What is process validation? Discover the meaning and importance of validation in the pharmaceutical industry. ✓ Learn ...
What is GxP Compliance?
Learn about GxP compliance in the pharmaceutical industry with Sware. Ensure regulatory compliance and quality ...
21 CFR Part 11 Basics: Connecting the Dots From Regulation to Compliance in the Life Sciences Industry
Learn the basics of 21 CFR Part 11 and how to connect the dots to GxP regulations and compliance in the pharma and life ...
Res_Q and AI: Modicus Prime Image Analysis for Quality Assurance
AI breakthroughs & pharmaceutical companies: Modicus Prime's CEO, Taylor Chartier, a leading AI expert, shares her ...
CSA vs CSV: What a Difference One Letter Can Make!
What is CSA vs CSV? Learn about computer software assurance vs computer system validation, and how CSA can help get you ...
Automating Software Validation: “Been There, Needed This”
Transforming life sciences compliance with superior client service. Sware's culture of care enhances value-added ...