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Medical Device Regulatory Affairs in Emerging Markets

Think Big: Strategic guidance for global regulatory success

Including APAC, Latin America, Russia & CIS, Africa & MENA

Regulatory Affairs in Emerging Markets Agenda Highlights

Taking you on a three-day regulatory world tour
  • Examine the updates and impact of regulatory reform across Asia Pacific
  • Explore the latest regulatory framework in the Middle East
  • Latin America: Ensuring device compliance in Brazil, Mexico and Argentina
  • Discover the latest progress of medical device regulation in Africa
  • Get to grips with the regulatory requirements in Russia, Turkey and the CIS
Connect with senior regulatory policy influencers from:
  • ANVISA
  • Malaysian Medical Device Authority
  • Turkish Ministry of Health
  • TUV SUD
  • Asian Harmonisation Working Party (AHWP)
Join insightful interactive discussions:
  • Best practice for successful product registrations in China
  • Navigating India’s regulatory processes for device registration
  • Sharing experiences of registering devices in ASEAN countries
  • Implementing Brazilian regulatory requirements for high-risk devices
  • How to develop an appropriate strategy for clinical conformity assurance across the CIS region

On-Demand Content

Speaker Interviews
Informative Articles

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