Remove keyword adverse-event-reporting
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Grand Rounds June 30, 2023: Decentralized Trials – From Guidance to Reality & What’s Left (Adrian Hernandez, MD, MHS; Pamela Tenaerts, MD, MPH; Craig Lipset, MPH)

Rethinking Clinical Trials

Additional considerations are needed for the data management plan, monitoring plan, safety plan, task log, and case report forms in the FDA draft guidance. What is your response to questions surrounding the issue of adverse event reporting issue ?

Trials 130
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The Transformative Power of Generative AI in eTMF: Enhancing Efficiency, Quality, and Compliance

Cloudbyz

Generative AI can employ natural language processing techniques to intelligently extract key data points, such as patient demographics, adverse events, and protocol deviations. Real-time Monitoring and Alerts: Generative AI can continuously monitor the eTMF for any critical events or anomalies.

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Grand Rounds March 17, 2023: Remote Symptom Monitoring with Electronic Patient-Reported Outcomes (ePROs) in Oncology (Ethan Basch, MD, MSc)

Rethinking Clinical Trials

Goldberg Distinguished Professor and Chief of Oncology Physician-in-Chief, North Carolina Cancer Hospital Director, Cancer Outcomes Research Program University of North Carolina Slides Keywords Patient-reported outcomes, Oncology, Clinical Trials Key Points Symptoms are common in cancer care. The culture has fundamentally changed.