It focuses on the role of the import managers when shipping
goods under the FDA and Customs Regulations. It also addresses what regulations
can be used to help the importer in understanding Automated Commercial
Environment (ACE) as the Sole CBP-Authorized Electronic Data Interchange (EDI)
System for Processing Certain Electronic Entry and Entry Summary Filings
Accompanied by Food and Drug Administration (FDA) Data. This review FDA
reporting criterion will influence the coordination transactions of your
company. The classification and valuation of the FDA goods for importing
purposes within their dutiable status and what are the proper documentation to
meet the country of origin requirements, and whether the FDA import
documentation meets the foreign law requirements.
This training event will provide guidance on how to access FDA agency documentation that will address the strict requirements of imports of goods for health and safety reasons. These regulatory requirements may influence the importer when it comes to the variety of product ingredients.
Key areas/ Benefits:
What are the importing ACE filing processes?
What are the Import FDA Agencies?
How are the FDA-Regulated Product procedures used within
the importation process?
What are the Customs Requirements?
Why are the administrative forms used in the importation
Explaining how to complete an EDI document in the importing
Define and describe the EDI with Customs Regulations. Why
is it considered a valuable automation tool for the FDA Regulatory process?
U.S. importers of FDA regulated products
New U.S. importers of FDA regulated products
Foreign exporters of FDA regulated products (companies
which sell regulated products to U.S. importers)
Purchasing department personnel for U.S. importers of FDA
Coordination/Supply chain managers and analysts
Trade regulatory/legislative affairs professionals
International business operations
Chief Executive Officers
Customs or Trade Compliance Personnel or Officers
Import or Global Trade Directors or Managers
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