Global Regulatory Requirements for U.S. Medical Device Exporters

The Global Healthcare Team will again feature FDAImports.com LLC, a Maryland-based consultancy agency, for an in-depth webinar that will provide 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. 

Cost: $38.00 USD

Note: This webinar is intended for U.S. Companies ONLY, incorporated under the laws of the U.S., with a product or service that has at least 51% U.S. content. This webinar is closed to press.