Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn moreDeveloping IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn moreDeveloping IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn moreDeveloping 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.
LEARN MOREReimagine 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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SEE LATEST REPORTSBy 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.
LEARN MOREBuilding 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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VIEW ROLESReal world evidence (RWE) is creating a new world of possibilities. Stakeholders across the healthcare ecosystem are recognizing the growing value of RWE across the product lifecycle. From regulators, payers, providers, and internal teams, RWE is informing decision making and driving value.
Join our upcoming conference to learn how you can demonstrate the value of your RWE strategies, and how it can be leveraged across stakeholders.
Exhibition / Networking
8:00AM – 9:00AM EDT
Session 1: The growing regulatory use of RWE
9:00AM – 10:00AM EDT
Real world evidence (RWE) can play an increasing role in complementing evidence from randomized clinical trials (RCTs) to support regulatory decision making. This session will explore how RWE is being used to fine-tune and extend the information value from RCTs, such as addressing the need for evaluating treatment benefits in populations that are underrepresented in RCT. We will also discuss lessons learned from both successful and unsuccessful attempts to use RWE for new drug approvals and label expansions, including how to determine whether real world data are sufficiently fit for purpose and emerging views on expectations for audit trails.
Session 2: How does RWE meet the value requirements from EU payers – now and in the future?
10:00AM – 11:00AM EDT
Health Technology Assessment (HTA bodies recognize the importance of Real World Evidence (RWE) to address uncertainties as they evaluate the effectiveness of new drugs. However, to date, RWE has had a limited impact on HTA decision-making. This panel with payer representatives will share their views on the impact of RWE today, and will discuss the path forward to increase the value of PRO data to inform HTA decision-making.
Session 3: Implementation Science – using RWE to drive impact for patients
11:00AM – 12:00AM EDT
Implementation Science is a means of introducing research findings and other evidence-based practices through strategically planned activities and data informed methods to improve the quality and effectiveness of routine practice within health services. Real world data helps to provide the evidence needed to drive change and benefit patients through evidence-driven healthcare delivery. This panel will showcase how new evidence and technology methods are aiding the adoption of evidence-based healthcare in the clinical setting, leading to better patient outcomes.
Exhibition / Networking
12:00PM – 13:00PM EDT
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