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1st Edition  Conference

Preparing for FDA's New Import/Export Trauma in 2020


"FDA’s new cost-saving import programs"
The FDA continues to change its import program to better manage new problems and to use new procedures to make the whole process easier. The FDA and U.S. Customs and Border Protection (CBP) are relying more and more on computer programs to expedite the import process. When and how you use these programs can make a big difference in the net profit derived from even a single shipment. The new Voluntary Qualified Importer Program (VQIP) is one such example. Another example is CBP’s and FDA’s implementation of the Automated Commercial Environment (ACE) program became mandatory for importers in 2016. If you fail to correctly use new import procedures and programs, you will be operating under an expensive disadvantage.

Highlights

  • Understand how U.S. Customs and FDA legal requirements intersect,Entry Process (U.S. Customs/FDA)
  • Learn how to mitigate and resolve import detentions,What happens when your product is detained?
  • What are the FDA’s import legal requirements and policy?,FDA’s new cost-saving import programs
  • You will be able to answer the following questions with this course without saying, “I don’t know?”
  • How do you deal with the FDA and the U.S. Customs and Border Patrol procedures?

Timings

8:30 AM - 4:30 PM (Oct 17) (General)
8:30 AM - 4:00 PM (Oct 18) (General)

Entry Fees

Paid Ticket Starts from 1899 USD View Details

Participants

20
Delegates

5 Exhibitors Estimated Count

Category & Type

Conference
Medical & Pharma
Education & Training

Editions

17-18 Oct 2019 1st Edition


Frequency Bi-annual
Next edition likely in Apr 2020 Interested

Official Links

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ComplianceOnline USA

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Visitor Ticket Price

1899 USDAttendee Seminar One Registration
32.777145 -96.806783

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