MOA Berlin,
Berlin, Germany
12 - 13 June 2024
OVERCOME ROADBLOCKS AND NAVIGATE A DIVERSE GLOBAL REGULATORY LANDSCAPE
Delve Into the Worlds Largest Medical Device Markets With Practical Case Studies to Accelerate Device Certification in the US and APAC
Training On US, China, Japan, Australia, AESAN Sovereign States, and South Korea with Experts from King & Spalding, Philips, Medical Technology of Australia & ARPA
Meet Your Global Device Regulatory Goals With Expert Insights
Navigate US Regulatory Requirements with Confidence
Immerse yourself in the latest US regulatory updates with our hands-on, 1-day workshop
Utilise the experience of King & Spalding and ISACA to accelerate device compliance
Deep dive into Q-submissions, 510(k)s, PMAs, and more!
Understand and Adhere to the Evolving APAC Landscape
Gain an understanding on requirements for China, Japan, Australia, Korea and ASEAN
Engage in practical case studies alongside trainers, Ed Woo & Jack Wong
Share experiences with other attendees on successful submissions within the region