Around the World: Regional Perspectives on the Regulation of AI and Software as a Medical Device
The International Bar Association (IBA) is hosting a webinar titled "Around the World: Regional Perspectives on the Regulation of AI and Software as a Medical Device." This event is scheduled for September 11, 2025, from 13:00 to 14:00 BST, and will be conducted online. The IBA, a leading global organization for legal professionals, aims to provide a platform for discussing the evolving regulatory landscape of artificial intelligence and software used as medical devices across different regions.
The webinar will delve into key topics such as the current regulatory frameworks governing AI and software as medical devices in various jurisdictions, challenges faced by regulators and industry stakeholders, and emerging trends in this rapidly evolving field. Discussions will also cover the impact of these regulations on innovation, patient safety, and market access.
Participants will have the opportunity to engage with experts in the field, including Yurika Inoue, who specializes in domestic and cross-border M&A within the pharmaceutical and medical device sectors, and Sanjeev Kumar Tiwari, an IP litigator with over 23 years of experience specializing in patent and design litigations. The session is designed to foster interactive discussions, allowing attendees to pose questions and share insights.
This webinar is particularly relevant for legal professionals, regulatory affairs specialists, compliance officers, and industry stakeholders involved in the development, regulation, and commercialization of AI and software as medical devices. Attending will provide valuable insights into regional regulatory perspectives, helping professionals navigate the complexities of global compliance and market entry strategies.
Speakers(3)
Beth Weinman
North American Regional Forum Liaison Officer, Healthcare and Life Sciences Law Committee at Ropes & Gray
Beth Weinman is a member of the firm’s life sciences regulatory & compliance practice group. She focuses her practice on FDA regulation and enforcement of laws governing pharmaceuticals, biologics, medical devices, cosmetics and dietary supplements. As a former lawyer with the U.S. Food and Drug Administration, Beth brings valuable perspective to clients who turn to her for representation in government investigations, assistance with internal compliance investigations, FDA enforcement actions, product recalls and other agency engagement strategies.
Sanjeev Kumar Tiwari
Asia Pacific Regional Forum Liaison Officer, Healthcare and Life Sciences Law Committee at K&S Partners
Sanjeev is Practice Chair, Litigation at K&S Partners. Sanjeev is an IP litigator with experience over 23 years and specializes in Patent and Design Litigations. Sanjeev's main areas of work involves litigation, patent invalidation, IP licensing & transnational and IP due diligences. Sanjeev is based out of New Delhi.
Yurika Inoue
Asia Pacific Regional Forum Liaison Officer, Healthcare and Life Sciences Law Committee at MORI HAMADA & MATSUMOTO
Yuri Inoue specializes in both domestic and cross-border M&A, while leveraging her graduate studies in medical devices and entrepreneurship to provide expertise in transactions such as M&A, licensing, collaboration, contract manufacturing and technology transfer, as well as related regulations, within the pharmaceutical and medical device sectors. Having lived extensively in the United States, Germany and Spain for a total of about 13 years, she is particularly skilled at managing cross-border projects. Her aim is to bridge cultural gaps and support companies in their international expansion and growth, ultimately contributing to their global business success.
Event Details
- Date
- September 11, 2025
- Location
- 🇬🇧 United Kingdom
- Pricing
- Unknown
- Audience
- Legal professionals, regulatory affairs specialists, compliance officers, industry stakeholders