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
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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Artificial intelligence is accelerating opportunities. Realizing the benefits for healthcare requires the right expertise. Together, we can solve the problems of today, and drive the breakthroughs of tomorrow.
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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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IQVIA enables genomic research via global access to a network of genomic-clinical data, proprietary technologies that enable federated analytics, and therapeutic area & bioinformatics expertise to help you answer your most pressing research questions.
LEARN MOREOur mission is to accelerate innovation for a healthier world. Together, we can solve customer challenges and improve patient lives.
LEARN MORECareers, culture and everything in between. Find out what’s going on right here, right now.
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"Improving human health requires brave thinkers who are willing to explore new ideas and build on successes. Unleash your potential with us.
SEARCH JOBSMeet the IQVIA Regulatory Intelligence team at this year’s RAPS Convergence, on
Booth 322. We will be showcasing our new user interface which will give you access to regulatory information for human drugs and biologics, medical devices and IVDs in over 100 countries, regions, and international organizations, where you can 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.
We will be presenting the following sessions:
Strategies for Holistic Labeling: Information Consolidation, Process Orchestration, Intelligent Automation & Resource Augmentation
Wednesday, October 4 | 12:05 – 12:35 pm
LOCATION : Exhibit Hall
Facilitator:
Cham Williams
Associate Director, Safety, Regulatory and Quality Solutions
Session Details:
Labeling is quickly becoming the forefront of data-centric processing in life science operations. As a result, a brighter spotlight is shining on the need to avoid noncompliance by optimizing labeling operations through advanced analysis and automation. Additionally, regulatory labeling requirements are continuously becoming stricter and more difficult to manage from both an intelligence and operational perspective. Companies and their regulatory teams are struggling to find a balance between the need to amend business processes and adopt new technologies in a way that is flexible and scalable while simultaneously minimizing cost.
Despite the challenges of balancing cost minimization with new technology adoption and process optimization, companies still face an immediate need to remain compliant in a challenging document-centric labeling environment. Companies desperately need to:
Managing regulatory change
Thursday, October 5, 2023 12:15 PM – 12:40 PM EDT
Spark Stage - #323
Speaker:
Bridget Wiseman
Director, Offering Management, Regulatory Intelligence, IQVIA
Session Details:
With a new or changed regulation being published every 21 minutes somewhere in the world, staying up to date with regulations is becoming increasingly more difficult. During this session we will look at some of the key trends and challenges; ways to manage the continual change in regulations, the impact on regulatory processes, keeping up to date and even influencing the regulatory landscape.
Topics:
• Understand the key trends in the regulatory landscape
• How to manage regulatory changes effectively
• The impact on regulatory processes
We look forward to seeing you there! Schedule a meeting with us today.
For more information on IQVIA Regulatory Intelligence, please visit this page.
Stay up to date with ever-changing regulatory requirements.
