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.
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Meet Your Market Access Goals in the US and APAC
Navigate US regulatory requirements with confidence
Day 4: 19 June 2025
Immerse yourself in the latest US regulatory updates with our hands-on, 1-day workshop
Deep dive into Q-submissions, 510(k)s PMAs, and more
Utilise the experience of the workshop leaders and accelerate device compliance
Understand and adhere to the evolving APAC regulatory landscape
Day 5: 20 June 2025
Navigate the varying medical device regulatory requirements for China, Japan, Australia, Korea and ASEAN
Engage in practical case studies with workshop leaders Ed Woo & Jack Wong
Share experiences with other attendees on successful submissions within the region