From manufacturing oversight to regulatory requirements, manage quality across your organization with a single enterprise software solution.


Are you prepared for the changes the EU AI Act will bring to the life sciences sector? This article explores the challenges and implications of the EU AI Act on the life sciences sector, particularly focusing on AI in medical devices and in-vitro diagnostics.
From manufacturing oversight to regulatory requirements, manage quality across your organization with a single enterprise software solution.
Outdated compliance practices aren't viable amid evolving market and regulatory changes.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.