Avoid Costly Delays and Master the FDA Import Process for Drugs and Devices.

Drug and device shipments are often delayed or denied entry into the U.S. due to issues like incomplete documentation, labeling mistakes, or active Import Alerts. For companies importing FDA-regulated products, a solid understanding of the import process—and how to effectively respond to detentions—is essential to maintaining supply chain continuity.

This webinar is designed to empower regulatory, quality, and supply chain professionals with critical insights into FDA procedures at the port of entry. You’ll learn how to respond to Notices of FDA Action, resolve detentions, secure shipment releases, and implement proactive strategies to prevent future compliance setbacks.

Gain expert-led, practical guidance to confidently navigate FDA import challenges and keep your products moving.