About The Webinar
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.
Speaker
DOMENIC J. VENEZIANO is an Independent FDA Regulatory and Strategic Consultant to Sandler, Travis & Rosenberg, P.A. He works closely with STR’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.
Key Topics
- Overview of food facility & dietary supplement facility registration requirements
- Overview of medical device establishment registrations and listing requirements
- Overview of cosmetic facility and product listing requirements s
- Key legal considerations and issues
