Introduction

Any medical device that is legally in the U.S. may be exported anywhere in the world without prior FDA notification or approval. The export provisions under section 802 of the FD&C Act only applies to unapproved devices. Devices that have not been approved or cleared in the U.S. must follow the export provisions of the FD&C Act. Foreign firms that manufacture medical devices and/or products that emit radiation that are imported into the United States must comply with applicable U.S. regulations before, during, and after importing into the U.S. or its territories.

Useful links

• Further event details More information about the event

Venue

OnlineTraining

OnlineTraining, 1000 N West Street, Delaware, Suite 1200, Wilmington, 19801, United States

Useful links

• Venue information More information about the venue

Organised by

GlobalCompliancePanel

Contact information

Mr webinars web
OnlineTraining, 1000 N West Street, Suite1200, DE, Wilmington, 19801, United States of America
8004479407
Contact us by email

---