Bioforum The Data Masters
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As 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...
On-demand
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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...
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Wednesday, July 24, 2024 · 10:00 AM EDTIntegrated summaries of efficacy (ISE) and safety (ISS) are required parts of NDA/BLA submissions as valuable tools for presenting and understanding the safety and efficacy of the product. Efficient and effective development of ISS and ISE involve...
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Tuesday, May 21, 2024 · 5:00 PM IDTWhen you think of a database lock, do you think of Data Management? Join us for a dynamic webinar exploring the intricate world of database lock processes and discover how Project Management plays a key role. You will learn proven PM strategies an...
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Tuesday, April 16, 2024 · 6:00 PM IDTDeveloping treatments for rare diseases pose many unique challenges that cannot be addressed by traditional study designs, including:
1) Prolonged enrolment periods and/or inability to enroll enough patients to formally power trials
2) Lack of c... -
Tuesday, February 6, 2024 · 10:00 AM KSTJoin Amanda Cross, Bioforum’s Chief Operating Officer, to learn how a data-first approach to outsourcing can speed your FDA submission timelines.
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Thursday, December 28, 2023 · 11:00 AM ISTThe webinar will be hosted in Hebrew
Join Limor Teomim and Ido Raz as they look at a strategic modernization approach to adapting computer system validation (CSV) to evolving technological landscapes define risks in software validation:
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Thursday, September 28, 2023 · 4:00 PM IDTJoin Sharon and Paul, Bioforum’s leading biostatisticians to discuss their experiences with the Risk-Based Quality Management (RBQM) and review of critical trial data. During the webinar we will demonstrate flexible strategies to support varying t...
