Clinical Data Talks
Podcast Description
Clinical Data Talks is your go-to podcast for an in-depth look at the evolving world of clinical data capture, management and analysis.
Join industry experts and clinical data enthusiasts as we explore the challenges, breakthroughs and innovations shaping the industry. Through fresh perspectives, real-world experiences and forward-thinking discussions, we keep you informed on the latest trends driving the future of clinical trials.
Whether you’re a data manager, researcher or passionate about the industry, Clinical Data Talks is your trusted source for insights into the world of clinical data.
Podcast Insights
Content Themes
The podcast focuses on the dynamics of clinical data capture, management, and analysis, with episodes covering the clinical data lifecycle, challenges in data management, and innovations in clinical trials. Specific examples include discussions on data fragmentation, interoperability, and the impact of emerging technologies on data workflows.
Clinical Data Talks is your go-to podcast for an in-depth look at the evolving world of clinical data capture, management and analysis.
Join industry experts and clinical data enthusiasts as we explore the challenges, breakthroughs and innovations shaping the industry. Through fresh perspectives, real-world experiences and forward-thinking discussions, we keep you informed on the latest trends driving the future of clinical trials.
Whether you’re a data manager, researcher or passionate about the industry, Clinical Data Talks is your trusted source for insights into the world of clinical data.
Applying real world evidence to clinical trials with Cristina Chang
In the final episode of season 1, Sylvain Berthelot welcomes Dr. Cristina Chang, Chief Medical Officer at HiRO, to unpack the growing importance of real-world evidence (RWE) in clinical development.
With decades of experience across global pharmaceutical companies, Cristina shares her deep insights into how real-world data is being applied to clinical trials to enhance patient outcomes, regulatory submissions, and post-marketing strategies. She discusses the practical considerations for using RWE, from data collection challenges to ensuring scientific rigor, as well as how the regulatory landscape is evolving to support these efforts.
Cristina also reflects on cultural and organizational changes needed to integrate RWE into clinical development successfully, and how emerging technologies and cross-functional collaboration can drive this transformation.
Join us as we explore how real-world evidence is shifting from a buzzword to a critical component of evidence generation in modern clinical research.
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