SmartSolve® now includes automated validation script authoring and execution
Streamline and manage your validation process with SmartSolve® Automated Validation Script Authoring and Execution.
Expedite script authoring and execution from weeks to days while improving quality with IQVIA SmartSolve® Automated Validation Script Authoring and Execution patented solution. Accommodate a more agile approach to enhancements so that you can adapt to change more efficiently and with increased accuracy.
- Shorten validation process from weeks to days
- Improve quality and eliminate human scripting errors
- Expand coverage to reduce risk without increasing staff and cost
- Take more frequent upgrades while reducing security risks
- Improve quality compliance with adherence to GAMP 5 standards/guidelines
Interested in learning more about SmartSolve’s Automated Validation Script Authoring and Execution capability? Let’s Talk.
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Transforming the Computer Systems Validation (CSV)
For Your QMS Through Automation
Computer systems validation (CSV) has long been a regulatory necessity but is considered time and resource-consuming to execute. Traditional Validation processes present challenges since they extend project timeline and costs, impacting time to market, resulting in an inability for life sciences organizations to promptly deploy newer versions of the software. Watch this webinar to learn how the utilization of automation can transform the CSV process for your QMS
See more innovation at IQVIA
Read this executive summary to learn about the value of adding automation to computer systems validation.
Shorten the SmartSolve validation process from weeks to days. Learn how in this fact sheet.
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