Import FDA in the Automated Commercial Environment (ACE) Authorized Electronic Data Interchange (EDI) System


Dr. Rossano V. Gerald is Keynote Speaker at Compliance key Inc he is an academic professor and founder of RVG International Consulting Firm, LLC. He has over thirty years of business experience in strategic management, marketing analysis, and supply chain management. Dr. Gerald is a veteran of the United States Army. He has worked with small and medium-sized businesses to help improve their business logistic processes through verification of operational and supply chain programs. Further, he has developed management and marketing strategies that were used to improve the efficiency and effectiv........

Overview

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 affect the logistics 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.

Why should you attend this webinar?

This training event provided guidance on how to access FDA agency documentations that are addressing the strict requirements of imports of goods for health and safety reasons. These regulatory requirements may affect the importer when it comes to the variety of product ingredients. For example, it will address the 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 by using reporting procedural and cases.

Areas Covered in the Session:

Who can Benefit:



Webinar Id: LSHCRG001

Training Options:

Duration: 60 mins

 View anytime

 Recorded: [Six month unlimited access]

 $237 (Single Attendee)  $599 (Unlimited Attendee)

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