Getting 'real' with real-world data: Discussing benefits & challenges of RWD in clinical trials
Join executive leaders from Walgreens, AbbVie, Cardinal, and Foley & Lardner Partners as they discuss how their organizations are using Real World Data (RWD) to move the needle on clinical trials to improve access to medications.
Today, clinical research, and the data collected within it, need to be more reflective of the real-world settings in which patients live, so that providers can better close care gaps and improve outcomes. As such RWD is playing an increasing role in healthcare and regulatory decision making, especially as the US Food and Drug Administration (FDA) is more open to accepting RWD to support its assessment of medical products. However, stakeholders lack a shared understanding of the FDA's expectations for the use of RWD in applications and research for new drugs and biologics.
As the healthcare and life sciences industry further develops common standards, structures and processes around RWD, consideration must be made to use cases that support the FDA's recent steps to increase racial and ethnic diversity in clinical trials.
Registration information
Event is open to: HBA Members and Nonmembers
Featured Speakers
Kim
Ribeiro
Head, Diversity and Patient Inclusion,
AbbVie Inc.
Ramita
Tandon
Chief Clinical Trials Officer,
Walgreens Boots Alliance
Aklilu
Tedla
VP, GM, Insights & Engagement, Regulatory Sciences, Advanced Therapy Solutions,
Cardinal Health
Pricing
| Regular Registration | $10.00 / €8.00 | $20.00 / €17.00 |
Members receive up to 50 percent discount
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