IQVIA SmartSolve Design Control streamlines medical device lifecycle management by providing centralized, policy-driven workflows for recording, reviewing, and approving design evidence. The solution integrates with document management, change management, and risk management modules to ensure compliance with regulatory requirements and maintain complete design history. Flexible templates, dashboards, and secure access help teams optimize productivity and demonstrate control over every phase of the design process.
Outdated compliance practices aren't viable amid evolving market and regulatory changes.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.
Explore how SmartSolve® eQMS for Pharma, an award-winning enterprise quality management system, seamlessly integrates quality into every aspect of life sciences operations. It empowers organizations to elevate quality standards, ensure regulatory compliance, accelerate time-to-market, and manage risks effectively.
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