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Outdated compliance practices aren't viable amid evolving market and regulatory changes.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.
Replace spreadsheets and disconnected tools with a single eQMS for deviations, audits, CAPAs, and approvals. SmartSolve® helps pharma teams maintain control, reduce compliance risk, and support regulatory readiness.
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 designed for Small Medtech and Pharma EBP. It automates CAPA, Deviation, Document, and Change Management, helping lean teams stay compliant while minimizing IT burden.
SmartSolve® RIM manages regulatory submissions, product registrations, and health authority interactions.
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