Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
"We strive to help improve outcomes and create a healthier, more sustainable world for people everywhere.
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Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster.
Research & Development Overview
Generate and disseminate evidence that answers crucial clinical, regulatory and commercial questions, enabling you to drive smarter decisions and meet your stakeholder needs with confidence.
REAL WORLD EVIDENCE OVERVIEW
Elevate commercial models with precision and speed using AI-driven analytics and technology that illuminate hidden insights in data.
COMMERCIALIZATION OVERVIEW
Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.
COMPLIANCE OVERVIEW
When your destination is a healthier world, making intelligent connections between data, technology, and services is your roadmap.
TECHNOLOGIES OVERVIEWExplore our library of insights, thought leadership, and the latest topics & trends in healthcare.
DISCOVER INSIGHTSAn in-depth exploration of the global healthcare ecosystem with timely research, insightful analysis, and scientific expertise.
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By making intelligent connections between your needs, our capabilities, and the healthcare ecosystem, we can help you be more agile, accelerate results, and improve patient outcomes.
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Building on a rich history of developing AI for healthcare, IQVIA AI connects the right data, technology, and expertise to address the unique needs of healthcare. It's what we call Healthcare-grade AI.
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Your new expert analyst is here. Be at the forefront of data-driven decision-making with a new generative AI tool that enables you to interact with our products and solutions like never before. Get results you can trust, faster.
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The IQVIA Human Data Science Cloud is our unique capability designed to enable healthcare-grade analytics, tools, and data management solutions to deliver fit-for-purpose global data at scale.
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The IQVIA Innovation Hub connects start-ups with the extensive IQVIA network of assets, resources, clients, and partners. Together, we can help lead the future of healthcare with the extensive IQVIA network of assets, resources, clients, and partners.
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IQVIA Decentralized Trials deliver purpose-built clinical services and technologies that engage the right patients wherever they are. Our hybrid and fully virtual solutions have been used more than any others.
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Empowering patients to personalize their healthcare and connecting them to caregivers has the potential to change the care delivery paradigm.
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"At IQVIA your potential has no limits. We thrive on bold ideas and fearless innovation. Join us in reimagining what’s possible.
VIEW ROLESMeet the IQVIA Regulatory Intelligence team at this year’s RAPS Convergence on booth #530. We will be showcasing our industry leading regulatory solution, which will give you access to regulatory information for human drugs and biologics, medical devices and IVDs in over 110 countries, regions, and international organizations. Here you will get the latest regulatory insights and real-time updates you need all in one place.
The RAPS Convergence is the largest and most recognized annual gathering of global regulatory affairs professionals and brings together representatives of industry, regulatory bodies, research, academia, and clinical organizations directly involved in managing the regulatory process and aligning science, regulation, and business strategy.
IQVIA Presents at RAPS
Empowering global regulatory affairs professional with automated surveillance solutions.
Speakers:
Michael King, Senior Director, Product Strategy, IQVIA
Bridget Wiseman, Director, Offering Management, Regulatory Intelligence, IQVIA
The range of global regulations and standards requiring monitoring can vary from company to company depending upon their target therapeutic area and product composition and, with the advent of software and AI embedded solutions, require regulatory affairs professionals to actively monitor an ever-increasing volume of content around the design, manufacture, sale, import, distribution, and post market activities. Failure to identify updated regulations and to meet the new requirements can result in fines and penalties, stop shipments and importation issues, and damage relationships with regulators and customers.
Supporting professionals with automated solutions for the tracking of global regulations and the creation of impact assessment plans can yield significant benefits by optimizing the ability to address regulatory change in real time and provide a single source of truth when tracking a company’s progress in meeting updated/ new regulation(s). Further enhancing end-to-end regulatory surveillance with Generative AI can increase the quality of remediation plans and timeliness of a company’s compliance to regulatory change.
Learning Objectives:
For more information on IQVIA Regulatory Intelligence, please visit this page.
Stay up to date with ever-changing regulatory requirements.
