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Think Global: Advance Your Medical Devices To New Regions With Leading Regulatory Knowledge And Know How

Regulatory Insights On China, APAC, LATAM, Russia & CIS, Japan, Canada And Beyond

Competent Authority Guidance And Industry Case Studies For Product Registration Around The Globe

2020 Highlights: Fast-track Medical Device Regulatory Registration For Global Success


Insider's Top Tips
Insider's Top Tips
  • Get regulatory updates on China, ASEAN and South Korea
  • Attain leading advice for device compliance in Brazil, Mexico, Argentina, Peru, Columbia & Chile
  • Explore registration strategies and requirements across EAEU, Pan-CIS & Russia
  • Discover the latest regulatory developments in Japan and Canada
  • Connect with senior regulatory policy influencers from Chinese NMPA, Brazilian ANVISA, Malaysian Medical Device Authority and TÜV SÜD 
Interactive Discussions
Interactive Discussions
  • Prepare your organisation for MDSAP in our panel discussion with ANVISA, BD, Berlin Heart and TÜV SÜD
  • Are you ready for change? ASAHI INTECC, Bioness, YURiA-PHARM evaluate the Global Impact of the EU MDR  
  • Manage your distributor regulatory risk with Synaptive Medical 
Elsewhere At The MedTech Summit...
Elsewhere At The MedTech Summit...
  • Attend our EU Medical Device Regulation track for comprehensive coverage of the latest regulatory guidance, case studies and lessons learned under the EU MDR
  • Gain leading insights into European software regulations in our Software & AI track
  • The FDA provide direct feedback on US combination product regulatory policy in our Drug Device Combination Products track
  • Join our EU IVD Regulation & Strategy track to hear how different countries & regions regulations compare
See The Full MedTech Summit Agenda