Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements 2015

  • 12 May 2015
  • Webinar

Description

Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements 2015 is a webinar that covers topics such as:

  • Introduction to FDA references and guidance documents related to import and export requirements
  • Import and export requirements for medical devices
  • Import Alerts
  • The regulatory process if you are a foreign manufacturer or initial importer and want to sell your device in the U.S
  • How to export unapproved and approved medical devices
  • Recordkeeping requirements and your responsibilities


Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements 2015 brings together attendees involved in design, project management, purchasing, production, servicing, installation, record keeping activities for medical device manufacturing and document control.

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Important

Please, check "Importing and Exporting Medical Devices: A Primer on Regulatory Strategy and Requirements" official website for possible changes, before making any traveling arrangements

Event Categories

Business: International Trade
Government & Global Issues: Law & Regulations
Health & Medicine: Medical device

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