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Developing Global Markets Healthcare
WEBINAR SERIES

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 1 Replay

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 2 Replay

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 

Webinar 3 Replay

Contact Us

Contacts: LeeAnne Haworth, Carey Esslinger, and Crystal Mills

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Global Business Navigator Chatbot Beta

Welcome to the Global Business Navigator, an artificial intelligence (AI) Chatbot from the International Trade Administration (ITA). This tool, currently in beta version testing, is designed to provide general information on the exporting process and the resources available to assist new and experienced U.S. exporters. The Chatbot, developed using Microsoft’s Azure AI services, is trained on ITA’s export-related content and aims to quickly get users the information they need. The Chatbot is intended to make the benefits of exporting more accessible by understanding non-expert language, idiomatic expressions, and foreign languages.

Limitations

As a beta product, the Chatbot is currently being tested and its responses may occasionally produce inaccurate or incomplete information. The Chatbot is trained to decline out of scope or inappropriate requests. The Chatbot’s knowledge is limited to the public information on the Export Solutions web pages of Trade.gov, which covers a wide range of topics on exporting. While it cannot provide responses specific to a company’s product or a specific foreign market, its reference pages will guide you to other relevant government resources and market research. Always double-check the Chatbot’s responses using the provided references or by visiting the Export Solutions web pages on Trade.gov. Do not use its responses as legal or professional advice. Inaccurate advice from the Chatbot would not be a defense to violating any export rules or regulations.

Privacy

The Chatbot does not collect information about users and does not use the contents of users’ chat history to learn new information. All feedback is anonymous. Please do not enter personally identifiable information (PII), sensitive, or proprietary information into the Chatbot. Your conversations will not be connected to other interactions or accounts with ITA. Conversations with the Chatbot may be reviewed to help ITA improve the tool and address harmful, illegal, or otherwise inappropriate questions.

Translation

The Chatbot supports a wide range of languages. Because the Chatbot is trained in English and responses are translated, you should verify the translation. For example, the Chatbot may have difficulty with acronyms, abbreviations, and nuances in a language other than English.

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