QCast: Data-Driven Dialogue in Drug Development
QCast by Quanticate is the podcast for biotech, pharma, and life science leaders looking to deepen their understanding of biometrics and modern drug development. Join co-hosts Tom and Jullia as they explore methodologies, case studies, regulatory shifts, and industry trends shaping the future of clinical research. Where biometric expertise meets data-driven dialogue, QCast delivers practical insights and thought leadership to inform your next breakthrough.
Podcasting since 2025 • 39 episodes
QCast: Data-Driven Dialogue in Drug Development
Latest Episodes
Episode 39: Automation in Clinical Trials
In this QCast episode, Jullia and Tom explore automation in clinical trials and why it matters for modern study delivery. They explain what automation looks like in day-to-day trial work, where it can reduce manual burden across consent, data f...
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Episode 39
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12:02
Episode 38: Observational Studies in Clinical Trials
In this QCast episode, Jullia and Tom explore observational studies and why they remain such an important part of the evidence base in drug development. They explain what makes an observational study different from an interventional trial, how ...
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Episode 38
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11:01
Episode 37: Phase 2b in Clinical Trials
In this QCast episode, Jullia and Tom explore phase 2b in clinical trials and why this stage plays such a decisive role in moving a programme towards phase 3. They explain how phase 2b is typically used to reduce uncertainty around dose, popula...
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Episode 37
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11:01
Episode 36: ACR Response Criteria in Rheumatoid Arthritis Trials
In this QCast episode, Jullia and Tom unpack ACR response criteria in rheumatoid arthritis clinical trials and why these endpoints are more operationally demanding than they look on paper. They explain what ACR20, ACR50, and ACR70 measure, how ...
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Episode 36
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11:08
Episode 35: Regulatory Submissions in Clinical Trials
In this QCast episode, Jullia and Tom explore regulatory submissions in clinical trials and why strong submission discipline protects timelines long before any scientific review begins. They discuss what a regulatory submission includes in prac...
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Episode 35
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11:16