You're Invited — Regional Challenges in Regulating Medical Product AI: A Discussion of the Different Regulatory Approaches in the US, EU, and UK

View email in browser INTZ et Al Webin'%fies / You're Invited – Regional Challenges in Regulating Medical Product AI: A Discussion of the Different Regulatory Approaches in the US, EU, and UK Join us for a discussion of recent legal and regulatory developments in the United States, the European Union, and the United Kingdom relating to the use of artificial intelligence in the life sciences industry. The participants will leverage their experiences with a wide range of digital health technologies and other clients to explore the similarities and differences in each region's approach to AI regulation, the impact of these approaches on industry stakeholders, and expectations for further AI legislation and regulation. The program will explore: * The evolution of AI regulation in the life sciences industry * Recent legislative initiatives, such as the EU's AI Act, and regulatory developments for AI * The effects of AI laws and regulations on pharmaceutical and medical device companies * Trends and expectations for future AI regulation and opportunities for advocacy When Wednesday, October 30, 2024 12:00 PM - 1:30 PM EST Where This is a virtual event, please register below to receive the Zoom link and add the event to your calendar. Register Here Panelists Alison Dennis Partner Taylor Wessing Alison Dennis co-heads the Life Sciences and Healthcare sector group of international law firm Taylor Wessing LLP. Alison has worked with medical device and digital health companies for more than 25 years and provides sophisticated advice in assisting companies to bring their products to market in Europe through quickly and commercially solving issues arising from regulations and with regulators.  M. Jason Brooke Managing Member & Attorney Brooke & Associates M. Jason Brooke, MSE, JD, CSQE is the Managing Member at Brooke & Associates—a digital health legal and regulatory advisory firm. Jason offers a unique, multi-disciplinary perspective on the digital health industry as a regulatory attorney, scientist, technologist, and quality compliance consultant. He brings a focused expertise in the medical device industry that combines more than 20 years of experience ranging from science and technology design, development, implementation, and testing, to business strategy and operations, to legal and regulatory compliance. Benjamin Zegarelli Of Counsel Mintz Benjamin Zegarelli, Of Counsel at Mintz, provides regulatory compliance counsel to global clients developing and marketing FDA-regulated products with the goal of mitigating compliance concerns and obstacles facing product candidates or commercialized products while helping clients achieve commercial success. With a clear focus on medical device compliance matters, Benjamin advises life science and health care industry clients on the federal and state laws governing the design, production, quality, and commercialization of a breadth of devices. Berooes [N Tayiorwessing Legal Regulatory » Quality + Compliance MINTZ