SMARTSOLVE® EQMS FOR PHARMA

Empower Your Team with AI-Enabled QMS to Achieve Faster, Safer Compliance

Streamline compliance, reduce risk, and accelerate innovation—delivering safe, effective medications faster.

Solutions Safety & Regulatory Compliance Quality Compliance QMS for Life Sciences | SmartSolve | AI- Enabled Compliance - IQVIA SmartSolve® eQMS for Pharma

SmartSolve eQMS

Transform your quality management and GxP

Drive a dual focus on patient safety and commercial performance.

The pharmaceutical industry is evolving rapidly and so are expectations for safer, higher-quality, and more innovative products. Implementing an enterprise Quality Management System (eQMS) isn’t just about keeping up, it’s about leading the way.

Experience the future of pharma quality, book a live demo of IQVIA's cutting-edge eQMS to transform your global GxP compliance.

Book a demo now

Quality Management Processes

Eliminate non-integrated data systems and streamline the management and execution of quality, regulatory and safety processes. Reduce risks, accelerate time to market for therapies, and enhance patient outcomes.

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

Compliant Processes

Quality is more than just a department; it is a company culture. Boost productivity and efficiency by maintaining compliance, bringing safe and effective products to market faster, and accelerating the journey toward a healthier world.

Change Management
Risk Management
Quality Portal
Complaint Management
SmartSolve Regulatory Connector
Postmarket Surveillance Module

Digital Content Management Processes

Whether you’re a small enterprise with fewer than 10 people or a large organization with thousands of employees, having scalable and well-defined processes is crucial. Effectively manage digital assets and ensure your team consistently works with the latest revisions by utilizing the following modules:

Change Management
Document Management
Quality Portal

Supplier Quality Management Processes

Supplier relationships are more crucial to quality management than often realized. They require strong trust, successful collaboration, and the ability to exchange expertise and resources. Streamline production, automate workflows, and unite data with end-to-end visibility into your supplier management.

Deviation Management
Nonconformance Management
Audit Management
Quality Portal
Inspection Management

FACT SHEET

Maximize Compliance. Minimize Risk.

Discover how an integrated eQMS can streamline quality processes, ensure regulatory compliance, and reduce risk across your organization.

Ready to see the benefits?

Download the fact sheet

REQUEST A DEMO

Ready to simplify compliance, reduce risk, and accelerate time-to-market?

Schedule a demo today and explore how a connected quality management system helps you optimize data, improve visibility, and make smarter decisions.

REQUEST A DEMO

SmartSolve eQMS Frequently Asked Questions

Get quick answers about SmartSolve’s quality management solutions, features, and best practices.

SmartSolve eQMS is designed to enhance your quality management processes. By streamlining data integration and automating manual tasks, it helps you reduce risks and accelerate time to market. For example, it offers modules for CAPA, deviation management, and quality event management, ensuring compliance throughout the product lifecycle. To learn more about how it can impact your operations, check out our SmartSolve eQMS overview.

SmartSolve offers a comprehensive suite of compliance management features. These include quality event management, audit management, and nonconformance management. Each module is designed to facilitate meticulous compliance with regulatory standards, making it easier for your organization to manage quality processes efficiently. Explore the features in detail in our factsheet.

Absolutely! SmartSolve is designed to be scalable. With solutions tailored for small biopharma companies, it automates essential processes like CAPA and document management, allowing smaller teams to maintain compliance without extensive IT resources. Discover more about our tailored solutions for biopharma here.

SmartSolve includes robust training and change management modules. These features ensure that your team is always up-to-date with the latest compliance standards and operational procedures. The platform allows for effective tracking of training completion and managing changes, thus minimizing disruption.

SmartSolve promotes seamless collaboration by integrating data and workflows. This eliminates silos within your organization, allowing teams to collaborate efficiently and make informed decisions quickly. It enables real-time access to data and insights, essential for maintaining compliance and operational efficiency.

SmartSolve is unique due to its industry-specific focus and modular flexibility. Tailored specifically for life sciences, it addresses the challenges faced by pharmaceutical companies, ensuring compliance and improving operational efficiency. Moreover, its modular design allows you to select only the features you need now and expand as your business grows.

Requesting a demo is simple! Just visit our website and fill out the demo request form. One of our experts will reach out to you to schedule a personalized demonstration, allowing you to see how SmartSolve can optimize your quality management processes. Start the process here.

IQVIA Technologies resources FROM IQVIA EXPERTS

Blog

CAPA Best Practice

Discover how the pharmaceutical industry can leverage CAPA to facilitate ongoing process enhancements.

White paper

Transforming The Computer Systems Validation (CSV) For Your QMS Through Automation

Massimo Franza, Anthony Hudson, and Davor Milosevic explore the benefits of incorporating automation into computer systems validation, highlighting the features of IQVIA's latest automated validation script authoring system within the SmartSolve solution.

Infographic

SmartSolve eQMS: Enhance quality and improve compliance throughout the product lifecycle

Mike King and industry experts discuss the challenges of data bias, accuracy, access, and the role of human involvement in AI for pharmaceutical development. Read their thoughts on data integrity, trustability, and explainability to ensure patient safety and effective regulatory compliance.

Blog

Understanding AI, Data and Human Interaction in Pharmaceutical Development

See how SmartSolve® eQMS improves compliance by automating and optimizing quality management processes, ensuring adherence to regulatory standards.

Explore More

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® 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® Fundamentals for EBP

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.