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Conference Details
FDA's New Import Program for 2018-Strict Precision
Date :
Place : Switzerland, Zurich
Contact Person:Paula Edwards
Description:
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.FDA's New Import Program for 2018-Strict Precision will be held in Zurich,Switzerland on date 2018-03-23
Deadline for abstracts/proposals : 21st March 2018
Organized By :New York Events List
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 re
Conference Highlights :Who will Benefit: The FDA’s regulatory controls for imported and exported devices have become increasingly pervasive and stringent. Foreign manufacturers, foreign exporters and domestic initial importers face greater scrutiny and are subject to expensive consequences if they do not plan carefully. Attendees need to understand the FDA’s and the US Customs Border Patrol’s regulatory criteria, inter-agency agreements and intra-agency procedures. The conference provides attendees with the o
Venue :Zürich, Switzerland
Check the event website for more details.
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