Mercure Hotel MOA Berlin, Berlin, Germany,
Hybrid Event I Attend In-Person Or Digitally
19 - 20 June 2025
Medical Device Regulatory Affairs in Global Markets: US and APAC
Delve Into The Worlds Largest Medical Device Markets. Unlock Certification Strategies. Accelerate Device Approval.
Meet Your Market Access Goals In The US And APAC
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 the workshop trainers to accelerate device compliance
Deep dive into Q-submissions, 510(k)s, PMAs, and more!
Understand and adhere to the evolving APAC regulatory landscape
Navigate the various medical device regulatory 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