Regulating AI-Based Medical Devices
Автор: APACMed
Загружено: 2021-04-29
Просмотров: 1648
This webinar was held live on Thursday, 25th June 2020. Healthcare is one of the industries that have the most to gain from the rise of AI, and the term "going digital" has become more and more synonymous with healthcare.
However, some imminent challenges must be overcome before physicians and other healthcare professionals can fully benefit from a digitized health ecosystem. Regulatory bodies have to re-imagine their approaches to AI regulation to fit the rapid, iterative nature of AI-based solutions. Integrated health data sets must comply with existing privacy laws like the EU's General Data Protection Regulation, and organisations must ensure data protection, transparency and cyber security.
The webinar was moderated by Varun Veigas from Roche Diagnostics, and had panelists Nathan Carrington from Roche Diagnostics and Lucas Nicolet-Serra from Simmons + Simmons to better understand what frameworks currently regulate AI and what is preventing the proliferation of AI, from industry and legal perspectives.
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