Seminar on Tougher Import Rules for FDA Imports in 2019

  • 2000.00 Dollar US$
  • Published date: February 15, 2019
    • Washington, Washington, United States

Course "Tougher Import Rules for FDA Imports in 2019" has been pre-approved by RAPS as eligible for up to 12 credits towards a participant's RAC recertification upon full completion.
Description:
FDA and the Customs and Border Patrol Service (CBP) have become increasingly sophisticated and equally demanding in the submission of import information and adherence to government procedures. Firms that fail to understand and properly execute an import and export program find their shipments delayed, detained or refused. As of December 2016, FDA and CBP officially implemented the Automated Commercial Environment (ACE) entry filing system. You either meet ACE requirements or face entry refusals and monetary penalties of up to $10,000 per offense. Other factors can derail the expectation of a seamless import entry process. The course covers detailed information about the roles and responsibilities of the various parties involved with an import operation and how to correct the weakest link(s) in the commercial chain. The course will include tips on how to understand FDA's thinking, negotiate with the FDA and offer anecdotal examples of FDA's import program curiosities.
Why you should attend:
What happens when your product is detained? FDA will begin a legal process that can become an expensive business debacle. You must respond fully within short timeframes. This is not the time for you to be on a learning curve. You need to have a plan in place and know what you are doing.
The FDA is steadily increasing the legal and prior notice information requirements. If you do not know what those requirements are and you initiate a shipment, your product is figuratively dead in the water. You must be accurate with the import coding information and understand the automated and human review process. If not, you can expect detained shipments. CBP is implemented a new "Automated Commercial Environment" computer program that changes import logistics and information reporting for FDA regulated products. Your shipment may be stopped before it is even loaded at the foreign port.
Who Will Benefit:
• Domestic importers
• Foreign exporter
• Initial importers
• International trade executives
• Venture Capitalists
• Marine insurance underwriters


Price:
1 ATTENDEE $2,000, Register for 1 attendee
5 ATTENDEES $10,000, Register for 5 attendees
10 ATTENDEES $20,000, Register for 10 attendees
Until March 10, Early Bird Price: $2,000.00
From March 11 to April 02, Regular Price: $2,200.00

Sponsorship Program benefits for seminar
For More Information- https://www.globalcompliancepanel.com/control/sponsorship


Contact us today!
NetZealous LLC DBA GlobalCompliancePanel
globalcompliancepanel@gmail.com
Toll free: +1-800-447-9407
Phone: +1-510-584-9661
Website: http://www.globalcompliancepanel.com

Registration Link - https://www.globalcompliancepanel.com/seminar/tougher-import-rules-for-FDA-imports-in-2019-901948SEMINAR?seo
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