Section 301 Tariffs: Updates & Resources
Section 232 Tariffs: Updates & Resources
IEEPA Tariffs: Updates & Resources
General Tariff Resources
Tariff stacking chart & information on how companies can respond to tariff increases.
Internationally recognized trade compliance training.
1 CCS / 1 CE Credit
Food facilities, dietary supplement facilities, medical device establishments, and cosmetic facilities and products are all subject to specific regulatory requirements by the Food and Drug Administration, but determining whether an item is regulated and must be registered can be confusing. However, failure to register can lead to detention or refusal of products upon import to the U.S. This webinar will highlight the differences between these products, clarify the existing regulatory landscape for medical foods and offer suggested compliance practices.
Contact webinarorganizers@strtrade.com if you have issues registering. Please note we do not take American Express
DOMENIC J. VENEZIANO is an Independent FDA Regulatory and Strategic Consultant to Sandler, Travis & Rosenberg, P.A. He works closely with ST&R’s FDA Practice Group to advise importers, exporters, producers, and distributors of commodities regulated by the Food and Drug Administration to ensure that they and their facilities comply with FDA laws and regulations.
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