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Harness the power to transform clinical development

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.

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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.

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Elevate commercial models with precision and speed using AI-driven analytics and technology that illuminate hidden insights in data.

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Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.

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THE IQVIA INSTITUTE

An in-depth exploration of the global healthcare ecosystem with timely research, insightful analysis, and scientific expertise.

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"Global Trends in R&D 2024

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Unlock your potential to drive healthcare forward

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 healthcare data deserves more than just a cloud.

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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Innovations make an impact when bold ideas meet powerful partnerships

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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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White Paper
Managing the Unexpected
How pharmaceutical organizations can use the unexpected to drive continuous improvement
Jul 08, 2019

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This paper shares best practices in EQMS and how to manage the unexpected to increase efficiency and reduce risk in future operations.

Unanticipated, unpredicted, unplanned, unexpected. These words can be undesirable descriptors of many actions or events, but among pharmaceutical quality and compliance professionals, they elicit downright fear.

In this environment, the occurrence of unexpected events signals that something in their organization’s processes or procedures is not completely under control and could possibly have a detrimental impact on product quality and patient safety. For this highly regulated industry, such occurrences not only carry risk, they have regulatory implications.

The FDA’s 21 CFR 211.192, states that any unexplained discrepancy must be investigated, and that the investigation will extend to all batches related to that issue, which can have a huge time and cost impact. EudraLex, The International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH), the World Health Organization (WHO), and other agencies around the globe have similar standards and guidances.

These pressures will only increase as regulatory bodies shift their focus beyond compliance to quality, and more specifically, to the sustainability of quality within pharmaceutical organizations. This means that an organization’s quality system needs to be built around the ability to identify and address the unexpected if they hope to meet regulatory expectations.

 

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