No more data discrepancies – just efficient collaboration and reduced risk
Focused industry expertise tailored to life science usage to support significant business impact.
Foster a commercially focused quality culture, efficiently manage complex processes and resources to meet tight deadlines and ensure compliance in a rapidly evolving global landscape.
Choose the solutions you need now and expand as your quality maturity, TA participation, or geographic reach increases.
Address all your quality compliance management needs from pre-market to post-market, including clinical trials, supplier management, manufacturing, and distribution.
Integrate data and workflows to automate manual, high-touch repetitive tasks, with compliance-specialized AI.
Drive a dual focus on patient safety and commercial performance.
Designed for quality professionals in pharmaceutical companies, IQVIA’s quality management software (eQMS software) addresses the challenges of establishing clinical, phase-appropriate quality processes and fostering a commercially-focused quality culture. It effectively manages complex processes, quality systems, and decision-making interdependencies, ensures efficient deployment of resources, and maintains compliance within both dynamic local ecosystems and broad global environments.
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.
|
|
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.
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:
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.
.png?mw=700&hash=F34EBF58AC095CE7EA47253AE8BCAE8C)
Discover how the pharmaceutical industry can leverage CAPA to facilitate ongoing process enhancements.
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.
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.
See how SmartSolve® eQMS improves compliance by automating and optimizing quality management processes, ensuring adherence to regulatory standards.
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.
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.
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.
.svg){kind=icon}
