SMARTSOLVE® EQMS FOR MEDTECH
Empowering Quality, Regulatory and Safety professionals to transform patient care
Improve productivity and efficiency throughout the lifecycle management process with an award-winning eQMS software
Improve productivity and efficiency throughout the lifecycle management process with an award-winning eQMS software
Accelerate market access and improve profitability with digital solutions that ensure cost-effective, timely compliance with evolving regulations and diverging standards.
Whether you are looking to deploy a few modules in a targeted solution or scale into a broader end-to-end ecosystem by deploying several eQMS modules with exponentially increasing benefits of automation and connectivity, IQVIA Quality Management Software can support companies of all sizes, from startups and SMEs to larger corporate organizations.
Ensuring compliance with regulations like FDA’s 21 CFR Part 820, ISO 13485, and EU MDR is crucial for successful commercialization. However, dealing with endless paperwork, navigating audits, and manually tracking traceability can be overwhelming. With efficiency designed specifically for MedTech, focus on what truly matters: improving more lives, faster. Connect your people, processes, and data under one single source of truth.
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Streamline and enhance your organization’s compliance programs while navigating complex MedTech regulations and regulatory changes. Align policies, standards, regulations, and controls to eliminate inefficiencies and redundancies.
With internal teams and supply chain partners more dispersed than ever, it's essential that everyone involved in new product development and introduction has easy access to the latest product and quality information. This ensures MedTech products are built as designed and delivered on time.
Whether you have a few partners or hundreds, our platform is designed for secure, rapid collaboration and traceability from early design through to volume production.
Effective content management enhances efficiency, ensures secure control and access, and reduces costs. Confidently manage digital assets—including text, images, videos, documents, and more—with seamless integration into IQVIA RIM Smart and IQVIA Regulatory Intelligence. Drive additional value across an end-to-end, connected ecosystem.
Listen to top regulatory and quality experts discuss factors that are driving regulatory change in the MedTech industry
Discover how a modular approach allows IQVIA end-to-end eQMS to be used in a way that scales with your company’s organizational growth and evolution.
Panelists discuss how IQVIA connected intelligence leverages social media and a quality management system to improve safety and early detection, enhance product surveillance, shorten cycle times by finding issues sooner, and improve regulatory compliance.
Discover how IQVIA RIM Smart transforms global MedTech compliance by consolidating and optimizing product registration activities.
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.
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.
IQVIA RIM Smart. Intelligence, automation and integration.
IQVIA SmartSolve® Fundamentals is a cloud-based QMS for small biopharma companies. It automates CAPA, Deviation, Document, and Change Management to ensure compliance with minimal IT resources.