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

Duration 60 Mins
Level Intermediate
Webinar ID IQW19A0136

  • How to report in the ACE to ensure CBP import compliance
  • Tips on processing Electronic Data Interchange (EDI) System for Processing
  • How to do Entry Summary Filings of FDA import products
  • 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 process
  • Explaining how to complete an EDI document in the importing process
  • Define and describe the EDI with Customs Regulations. Why is it considered a valuable automation tool for the FDA Regulatory process

Overview of the webinar

This training event provides guidance on how to access FDA agency documentation that are addressing 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. 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. It also addresses what regulations can be used to help the importer in understanding FDA guidelines by U.S. Port of Entry requirements developed and developing markets.

 

Who should attend?

  • Company Executive Officer (CEO)
  • Entrepreneurs 
  • Distributor Channel Managers 
  • Health Service Providers
  • Wholesalers Perishable Goods
  • Grocery Retailers 
  • Logisticians

Why should you attend?

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 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.

 

Faculty - Dr. Rossano Gerald

Dr. Gerald is an Academic Professor and Founder of RVG International Consulting Firm, LLC. He has over 25 years of business experience in, strategic management, marketing analysis, and supply chain management. Dr. Gerald worked with small and medium-sized businesses to help improve their business logistic processes through verification of operational and supply chain programs. Also, he had developed management and marketing strategies that were used to improve the efficiency and effectiveness of his client business operations in this global economy. 
 
He earned a Doctor of Business Administration in International Business and Advanced Professional Business Certification in Marketing from Argosy University/Sarasota; He also holds a Master of Science of Law (J.S.M.) degree and a certificate in Compliance & Risk Management from Thomas Jefferson School of Law in International Tax and Finance Services. He graduated with MBAs degrees in Project Management degree from the University of Phoenix and Webster University in Business Administration. He also earned a Graduate Certificate in Supply Chain Management at Penn State’s Smeal College of Business MBA Program. He is also a Certified Professional Coach (American Public University System).

Dr. Gerald is also a member of the Free Trade Alliance, San Antonio Transportation Association, Inc., San Antonio SCORE, TX, Supply Chain Council and Institute of Business Forecasting & Planning, and CATO Institute of Research & Analysis and Academy of Business Research. He is a Certified Supply Chain Manager, and Inventory Planner and Property Forecaster, Certified Consultant for Business Value Analysis and Methodology, Certified Export Leaders of the Free Trade Alliance and Casa of San Antonio, TX; Certified Master Management Consultant and Master Project Manager; and Certified Marketing Analyst and Registered Business Analyst by the International Management Consultant Certification Board (IMCB). 

 

Certified CCA ™ Chartered Compliance Analyst AAFM ® American Academy of Financial Management/ Certified International Project Manager (CIPM) of the AAPM ® American Academy of Project Management. A member of the Council of Supply Chain Management Professionals; and an Advisor for the Mu Kappa Tau Marketing of the Honor Society. He has published scholarly papers in the Journal of International Business and Economics and the Strategic Management Quarterly.

 

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