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IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise.


IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 79,000 employees, IQVIA conducts operations in more than 100 countries.

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MedTech Market Access Trends: Design for Registration – Principles of a Global Approach

Download your free webinar summary to capture key insights into overcoming challenges such as: Discover the critical importance “design for registration” or “manufacture for compliance” plays in optimizing global product launches.
Whitepaper Clinical Studies Pharmaceutical Research and Development
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UDI Requirements: The Fear of the Unknown

Understand the function of UDI and access key takeaways on improving processes surrounding it, in your summary of a recent insight-packed webinar. Capture valuable information on how your organization can better manage the complex and often conflicting regulatory environment you may be facing when designing your UDI systems and workflows. Access the highlights and critical insights from “UDI Requirements: The Fear of the Unknown,” a recent webinar from Citeline’s MedTech Insight, presented in partnership with IQVIA Technologies. Discover how a comprehensive, single-source-of-truth UDI solution can support you in overcoming your country-specific operational challenges.
Whitepaper Clinical Studies Pharmaceutical Research and Development
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Pharma Intelligence UK Ltd logo
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MedTech Market Access Trends: Embracing Change and Dealing with It

Discover how you can maintain your focus on patient safety, market access, and commercial success with strategies for creating change management systems that facilitate regulatory intelligence sharing, cross-functional alignment, and efficiency.
Whitepaper Clinical Studies Pharmaceutical Research and Development