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

Posted By : User Ref No: WURUR68731 0
  • Image
  • TypeSeminar
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  • Location Los Angeles, California, United States
  • Price
  • Date 17-11-2020 - 18-11-2020
Seminar Title
Preparing for FDA's New Import/Export Trauma in 2020
Event Type
Seminar
Seminar Date
17-11-2020 to 18-11-2020
Location
Los Angeles, California, United States
Organization Name / Organize By
complianceonline
Organizing/Related Departments
Sales & marketing
Organization Type
Event Management Company
SeminarCategory
Technical
SeminarLevel
All (State/Province/Region, National & International)
Related Industries

Business Development

Finance

Manufacturing

Export/Import

Shipping/Marine

Location
Los Angeles, California, United States

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.

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Registration Fees
Not Mention
Registration Ways
Email
Address/Venue
  6201 America Center Drive Suite 240 San Jose, CA 95002, USA 
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