Cross-Border Insights: Navigating UK/EU Regulations and US Exclusivities in Medtech and Healthtech

Global growth in life sciences demands a clear understanding of regulatory landscapes on both sides of the Atlantic. This webinar will bring together insights on navigating evolving UK/EU medtech and healthtech requirements and demystifying the complexities of US regulatory exclusivities—helping companies streamline compliance, unlock protections, and maximize market opportunities.

Wolf Greenfield’s Jon Roses will present on “Exclusivities for and Regulation of Medical Devices and Diagnostics in the US,” while Martin Becker, Regulatory Lead, HealthTech at Centre for Process Innovation (CPI) will present on “Navigating the UK and EU Regulatory Landscape for Medtech & Healthtech Companies.”