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 and FDA implementation of the Automated Commercial Environment (ACE) program became mandatory for importers in 2016. If

Date : 24th August 2017 to 25th August 2017

Place : United States, Philadelphia

Website :https://www.eventbrite.com/e/fda-new-import-program-for-2017-strict-precision-com-tickets-33414036282?aff=NDT

Contact Person:Paula Edwards

Description:

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

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 and FDA implementation of the Automated Commercial Environment (ACE) program became mandatory for importers in 2016. If will be held in Philadelphia,United States on date 2017-08-25

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Deadline for abstracts/proposals : 1st August 2017

Keynote Speakers : Casper (Cap) Uldriks Former Associate Center Director of FDA's CDRH Casper (Cap) Uldriks, through his firm “Encore Insight LLC,” brings over 32 years of experience from the FDA. He specialized in the FDA’s medical device program as a field investigator, served as a senior manager in the Office of Compliance and an Associate Center Director for the Center for Devices and Radiological Health. He developed enforcement actions and participated in the implementation of new statutory requ

Conference Highlights :FDA’s new cost-saving import programs Understand how U.S. Customs and FDA legal requirements intersect Know how to manage foreign suppliers Understand FDA’s internal procedures Learn how to mitigate and resolve import detentions Learn how to avoid common problems Develop practical ways to improve your import and export business You will be able to answer the following questions with this course without saying, “I don’t know?” What are the FDA’s import legal requirements and p

Venue :Philadelphia, PA, United States

Check the event website for more details.