A strong Corrective and Preventive Action (CAPA) program is critical for ensuring quality and regulatory compliance. Inadequate CAPA documentation is a leading cause of FDA 483 observations, which can damage your brand and even lead to shutdowns. Access the infographic to discover best practices for building an effective CAPA workflow.
Outdated compliance practices aren't viable amid evolving market and regulatory changes.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.
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.
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.
.svg){kind=icon}
