This Webinar will provide a broad overview of the requirements and expectations and an introduction to the regulations, including 21 CFR 1, Subpart E--Imports and Exports. Entry information should identify the product and include appropriate information to demonstrate that the product is in compliance with FDA regulations.
Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements - Webinar by GlobalCompliancePanel
20 February 2014, Fremont, United States
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Online Event
Online Event, 161| Mission Falls Lane| Suite 216, Fremont| CA 94539, Fremont, 94539, United States
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GlobalCompliancePanel
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