Exploring Emerging Regulatory Trends in APAC and South AmericaEducation Sessions<img alt="" height="200" src="https://assets.swoogo.com/uploads/medium/3515330-65c260b7b0019.jpg" style="margin:10px;float:right;" width="300" /> The global medical device regulatory landscape is a complex tapestry, and staying abreast of updates beyond the U.S. and EU can be challenging. This session empowers you to focus on emerging trends in key APAC and South American markets. Join industry experts for a comprehensive overview of the APAC regulatory landscape. Gain insights into evolving regulatory frameworks in Australia and other key APAC markets, including updates on registration requirements, clinical trial regulations and postmarket surveillance. You’ll also learn how to navigate the dynamic regulatory environment in Brazil, Argentina and other major South American markets with an understanding of specific requirements and upcoming changes. Head home from this session with ways to identify opportunities and challenges posed by these evolving regulations and develop informed strategies for successful market entry and expansion. Learn from the practical experiences of companies that are successfully navigating regulatory hurdles in APAC and South America. Don’t miss out on critical regulatory updates shaping the future of medical device access. This session equips you with the knowledge and connections you need to navigate the evolving APAC and South American regulatory landscape with confidence. This session is presented in collaboration with the Orthopaedic Surgical Manufacturers Association (OSMA), a device-company-led organization that works to enhance the implementation of global regulations and foster productive interactions between the orthopedic industry and regulators.

Description

The global medical device regulatory landscape is a complex tapestry, and staying abreast of updates beyond the U.S. and EU can be challenging. This session empowers you to focus on emerging trends in key APAC and South American markets.

Join industry experts for a comprehensive overview of the APAC regulatory landscape. Gain insights into evolving regulatory frameworks in Australia and other key APAC markets, including updates on registration requirements, clinical trial regulations and postmarket surveillance. You’ll also learn how to navigate the dynamic regulatory environment in Brazil, Argentina and other major South American markets with an understanding of specific requirements and upcoming changes. Head home from this session with ways to identify opportunities and challenges posed by these evolving regulations and develop informed strategies for successful market entry and expansion. Learn from the practical experiences of companies that are successfully navigating regulatory hurdles in APAC and South America.

Don’t miss out on critical regulatory updates shaping the future of medical device access. This session equips you with the knowledge and connections you need to navigate the evolving APAC and South American regulatory landscape with confidence.

This session is presented in collaboration with the Orthopaedic Surgical Manufacturers Association (OSMA), a device-company-led organization that works to enhance the implementation of global regulations and foster productive interactions between the orthopedic industry and regulators.