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

SMARTSOLVE

Improve patient outcomes and company performance

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.

Maximize audit performance with a patient focused compliance strategy

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.

  • Training Management
  • Change Management
  • CAPA Management
  • Deviation Management
  • Nonconformance Management
  • Audit Management
  • Quality Event Management
  • Quality Intelligence
  • Risk Management
  • Asset Management
  • Design Control Management
  • Quality Portal
Protect your brand and reputation: minimize risk of compliance violations

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.

  • Change Management
  • Risk Management
  • Quality Portal
  • Complaint Management
  • SmartSolve Regulatory Connector
  • Postmarket Surveillance Module
Optimize supply chain alignment and performance

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.

  • Deviation Management
  • Nonconformance Management
  • Audit Management
  • Quality Portal
  • SmartSolve Regulatory Connector
  • Inspection Management
Deliver the right content to the right audience at the right time

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.

  • Change Management
  • Document Management
  • Quality Portal

Fact sheet

Enhance performance across the whole product lifecycle

Discover how IQVIA’s end-to-end eQMS for MedTech streamlines quality and regulatory compliance, transforming your people, processes, and data into a centralized hub.
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