Developing Global Market Pathways for U.S. Medical Device Exporters Webinar Series
Developing Global Market Pathways for U.S. Medical Device Exporters Webinar Series
The U.S. Commercial Service’s Global Healthcare and Health Tech Team has arranged a 3-part webinar series for new and seasoned exporters to help develop their export strategy when selling medical devices and diagnostic companies to international markets. Topics will cover core concepts of market access, U.S. Food and Drug Administration (USFDA) requirements for exporting, and regulatory pathways for select countries.
Webinar 1: Overview of U.S. Food & Drug Administration Regulatory Requirements for Exports
New-to-export companies and seasoned exporters would benefit from this webinar to learn about U.S. Food and Drug Administration (USFDA) export requirements for U.S. medical device exporters
This webinar features FDAImports.com LLC, a Maryland-based consultancy agency, for an in-depth webinar that will provide an overview of the USFDA regulatory requirements for exporting medical products from the United States to other countries. This session includes a review of general requirements for medical products and how they interact with export requirements as well as unique requirements imposed by USFDA on exporters.
- Recorded on January 17, 2024
- Replay Cost: $38
Webinar 2: Global Regulatory Requirements for U.S. Medical Device Exporters
The Global Healthcare Team features FDAImports.com LLC, a Maryland-based consultancy agency, for an in-depth webinar that provides a broad overview of the main regulatory pathways available in the European Union (“EU”), Health Canada, Australia, and Mexico to help companies strategically plan for pre- and post-marketing activities for medical products in these markets.
- Recorded on January 24, 2024
- Cost : $38
Webinar 3: Navigating Global Market Access for U.S. Medical Device & Diagnostic Companies
Join the Global Healthcare Team and Avania market access for an in-depth webinar focused on the core concepts of global market access for U.S. medical device and diagnostic companies. This webinar will help U.S. exporters understand how to qualify healthcare markets using a combination of clinical and economic data and local market factors with a specific focus on European single payer systems and comparable systems in Canada, the EU, and Mexico. U.S. medical device companies will learn how to prepare for—and navigate—these pathways. Whether you are a seasoned exporter or new to global market expansion, this webinar will equip you with the knowledge to succeed in the global healthcare market.
- Recorded: February 7, 2024
- Cost: $38
Contact Us
Contacts: LeeAnne Haworth, Carey Esslinger, and Crystal Mills