SmartSolve® Automated Validation and Extended Validation Services revolutionize computer system validation for life sciences organizations by automating script authoring and execution, reducing project timelines from weeks to days. This patented solution streamlines the entire validation process, eliminates manual errors, and enables more frequent software upgrades while maintaining compliance with GAMP 5 standards. With managed and extended service options, organizations can expand coverage, minimize risk, and optimize resources, all within an AI-enabled, Microsoft Azure-based platform designed for global quality management and regulatory compliance.
Outdated compliance practices aren't viable amid evolving market and regulatory changes. IQVIA’s award-winning, end-to-end quality management system streamlines the product value chain, accelerates market entry, safeguards companies and patient safety, and meets complex regulatory demands.
Explore how SmartSolve® eQMS for Pharma, an award-winning enterprise quality management system, seamlessly integrates quality into every aspect of life sciences operations. It empowers organizations to elevate quality standards, ensure regulatory compliance, accelerate time-to-market, and manage risks effectively.
Discover how an end-to-end eQMS solution empowers QARA professionals to remain agile, well-informed, and proactive in ensuring the safety and efficacy of medical devices.
IQVIA SmartSolve® Fundamentals is a cloud-based QMS for small biopharma companies. It automates CAPA, Deviation, Document, and Change Management to ensure compliance with minimal IT resources.
SmartSolve® RIM manages regulatory submissions, product registrations, and health authority interactions.
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