AI in Change Management: A Key Enabler for Data‑Driven MedTech

This white paper explores how Artificial Intelligence is transforming change management in medical device manufacturing and regulatory registrations by enabling data‑driven, audit‑ready decision‑making. It examines AI‑enabled change control across quality and regulatory (QARA) processes, including predictive impact analysis, digital traceability, and governance within modern eQMS platforms. Designed for MedTech leaders, the paper provides practical insights to improve compliance, reduce regulatory risk, and accelerate global product changes.

SmartSolve® eQMS for Lifesciences

Outdated compliance practices aren't viable amid evolving market and regulatory changes.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.

SmartSolve® eQMS for MedTech

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.

SmartSolve® RIM

SmartSolve® RIM manages regulatory submissions, product registrations, and health authority interactions.

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