Bioforum The Data Masters
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The regulatory environment for clinical trial reporting has changed significantly in recent years, creating new expectations for medical writers, regulatory affairs professionals, and clinical operations teams.
This webinar will provide a clear, ...
This webinar will provide a clear, ...
On-demand
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Wednesday, July 8, 2026 · 10:00 AM EDTAI is now appearing across the clinical trial lifecycle; from protocol planning and feasibility to site selection, data review, reconciliation, patient-facing technologies, oversight, and reporting. But for many clinical trial teams, the real chal...
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Tuesday, July 7, 2026 · 9:00 AM EDTImportant note: To maintain a focused and interactive format, live attendance is limited and registration is subject to approval.
As protocol writing moves from narrative drafting toward structured, machine-readable content, ICH M11 is re... -
Wednesday, June 10, 2026 · 10:00 AM EDTA proposal can look complete on paper, but the real test comes when the study moves into delivery.
Assumptions around scope, timelines, responsibilities, data complexity, outputs, review cycles, and resourcing can all seem clear at the proposal ... -
Tuesday, April 28, 2026 · 10:00 AM EDTJoin us for a clear, engaging walkthrough of the fundamentals of clinical study design, grounded in ICH E8 principles. We’ll explore study phases, prospective vs. retrospective approaches, controlled vs. uncontrolled trials, and key interventional...
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Tuesday, March 31, 2026 · 10:00 AM EDTJoin Bioforum and CCS for a practical discussion on adaptive and Bayesian trial designs and the endpoint choices that can make or break cardiovascular studies. We’ll cover key tradeoffs, common pitfalls, and lessons learned across time-to-event, e...
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Thursday, February 26, 2026 · 9:00 AM ESTAs the estimand framework becomes standard across clinical trials, “per-protocol” analyses are being re-examined for what they truly estimate and whether it is needed when the intercurrent event strategies address its elements. In this Bioforum we...
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Wednesday, November 12, 2025 · 11:00 AM ESTThe FDA’s Project Optimus is transforming how oncology drug developers approach dose selection — shifting the focus from identifying the Maximum Tolerated Dose (MTD) to optimizing for both efficacy and patient safety. This new paradigm directly im...
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Tuesday, October 28, 2025 · 9:00 AM EDTAdopting Risk-Based Quality Management (RBQM) can make or break clinical trial success — and the CRO you choose plays a crucial role. Yet, moving from theory to effective implementation is rarely straightforward.
Join us for a live, interactive di... -
Monday, June 23, 2025 · 6:00 PM IDTAs clinical trials grow more complex, study teams face increasing challenges in managing data quality, integration, and regulatory compliance. The use of AI and machine learning (ML) is transforming how clinical data is collected, analyzed, and ac...
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Wednesday, May 7, 2025 · 4:00 PM IDTDiscover how to align your trial strategy with FDA’s Project Optimus, from understanding the initiative to implementing smart trial designs and effective data analysis. Get the insights you need to stay ahead in oncology drug development.
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Wednesday, February 26, 2025 · 4:00 PM ISTAs AI continues to evolve, its impact on biostatistics and statistical programming in clinical trials is becoming increasingly significant. This webinar will explore emerging trends, the integration of AI-driven tools, and how they are shaping da...
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Tuesday, January 28, 2025 · 5:30 PM ISTJoin experts in the medical writing field for an insightful webinar on AI tools. This session will explore how AI enhances efficiency and accuracy in medical writing, key strategies for integrating AI into workflows, and the ethical considerations...
