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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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.
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 JOBSFor biopharma companies looking to ensure proper lifecycle management for their therapeutic, it is critical to design an adept regulatory strategy as early as possible. Depending on a company’s budget, internal capabilities, and regulatory experience, they may opt to develop their regulatory strategy in-house or collaborate closely with a regulatory service provider to identify where they can implement technology like artificial intelligence (AI), machine learning (ML), natural language processing (NLP), and language learning models (LLMs) to improve accuracy, efficiency, and regulatory compliance across their processes. If your team is considering how best to tailor your regulatory strategy, consider the emerging trends and best practices across the industry that may help guide your approach.
Developing a regulatory approach as early as possible can help your team adapt and respond to challenges more efficiently. Consider the following benefits:
The pathway to enhancing reliability and efficiency requires embracing technology and process improvement. For lifecycle management activities, which involve multiple regulatory submissions, different product types, and various countries, it is critical to ensure that standardized processes and up-to-date regulatory intelligence are used. To stay ahead of the curve for your lifecycle management goals, explore the trends emerging across the biopharmaceutical industry:
In a recent panel discussion on lifecycle management and regulatory strategy, IQVIA Leaders, Marcela Miño, Senior Director and Global Head of Lifecycle Management; Rama Mohan Rao Chikkam, Senior Director of Global Regulatory Operations and APAC RA; Keith McDonald, Head of Drug Development Strategy; and David Cameron, Senior Director and Global Group Head, Novel Trial Design Solutions, discussed emerging trends in lifecycle management, labeling, and publishing, and how drug developers are adapting their regulatory strategies to accommodate them. To learn more, download the full white paper, The Future of Regulatory Operations.
Meet the challenge of changing stakeholder demands and increasing cost constraints with IQVIA's integrated technology services and analytics-driven offerings.
Automate and standardize your regulatory management, from correspondence and commitments to registration and tracking.
Reimagine regulatory service delivery.
