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
Meet the speakers:
On-Demand Content
Speaker Interviews
Speaker Interview with Marina Semenova, QA Manager, Arkray, Russia
*2019 SPEAKER INTERVIEWS COMING SOON*
Informative Articles
*NEW ARTICLES COMING SOON*