Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements - Webinar By GlobalCompliancePanel

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Areas covered in the session:
Examine the import and export requirements for medical devices
Introduction to FDA references and guidance documents related to import and export requirements
Understand the regulatory process if you are a foreign manufacturer or initial importer and want to sell your device in the U.S.
Import Alerts
Recordkeeping requirements and your responsibilities
How to export unapproved and approved medical devices
Who will benefit: This webinar will provide valuable assistance and guidance to device companies involved in importing and exporting of medical devices. Employees who will benefit include:
All levels of management and departmental representatives and those who desire a better understanding or a "refresh" overview of the export/import process
Regulatory Affairs
Clinical Affairs
Quality and Compliance
Marketing & Sales
Distributors/Authorized Representatives
Engineering/Technical Services/Operations
Consultants