Outdated compliance practices aren't viable amid evolving market and regulatory changes.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.
IQVIA SmartSolve® Risk Management streamlines product- and process-based risk assessments with guided, methodology-driven workflows for FMEA and PHA. The solution helps medical device and IVD manufacturers improve consistency and traceability across risk identification, evaluation, mitigation, acceptance and reporting, while supporting ISO 14971:2019-based risk management, audit readiness and regulatory compliance.
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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.
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.
