Register Now: Beyond EDC: Designing a Connected Data Strategy for Predictive Clinical Development
Blog|Articles|December 24, 2024

Our Top 5 Most Viewed Conference Video Interviews of 2024

Applied Clinical Trials sat down on-site with many KOLs at some of industry's largest gatherings in 2024 including SCOPE, DIA, and DPHARM.

Below is a list of the most viewed video interviews from Applied Clinical Trials' on-site conference coverage in 2024.

1. DIA 2024: Ginny Beakes-Read of Johnson & Johnson Discusses Regulatory Challenges

In an interview at DIA 2024, Beakes-Read, head, global regulatory policy and intelligence, Johnson & Johnson Innovative Medicine highlights the integration of technological advancements into drug development and benefits patients are seeing from FDA's Accelerated Approval Program.

Watch the interview here.

2. DPHARM 2024: Acclinate CEO Del Smith Highlights the Roles of Technology and Engagement in Clinical Research

In an interview at DPHARM 2024, Smith discusses how predictive modeling and community engagement can increase diversity.

Watch the interview here.

3. SCOPE 2024: Steve Young of CluePoints Discusses RBQM and Key Risk Indicators

In an interview at SCOPE, Young, Chief Science Officer, CluePoints discusses where the industry is currently adopting RBQM and the level of comfort that comes with it.

Watch the interview here.

4. SCOPE 2024: YPrime CEO, Jim Corrigan Speaks About the Company and Addressing Uncertainty in Clinical Trials

In an interview at SCOPE, Corrigan discusses what YPrime is doing to address challenges in clinical trials and results from the company's recently released eCOA report.

Watch the interview here.

5. DIA 2024: Rob DiCicco of TransCelerate Biopharma Discusses the State of AI in Clinical Research

In an interview at DIA 2024, DiCicco, vice president, portfolio management, TransCelerate Biopharma highlights the use of artificial intelligence in clinical research from the perspectives of different stakeholders.

Watch the interview here.


Related to this article

What Needs to Happen Beyond the Clinical Trial Modernization Act
In this video interview, Kent Thoelke, CEO of Paradigm Health, calls for safe harbor protections, CMS reimbursement safeguards, and funding mechanisms modeled on EHR meaningful use to help community and rural institutions participate in research on par with academic centers.
Building AI Assistants Clinical Trial Teams Can Trust: Q&A with E.K. Koh, Suvoda
In this Q&A, E.K. Koh, chief product officer at Suvoda, discusses what separates a trustworthy AI assistant from one that adds risk, why curated clinical knowledge matters more than general-purpose flexibility, and what safeguards must be in place when assistants move from answering questions to taking actions in clinical trial systems.