ComplianceOnline

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

Instructor: Rossano V Gerald
Product ID: 705212
  • Duration: 60 Min
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Read Frequently Asked Questions

This FDA import webinar 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 procedures and cases.

Why Should You Attend:

This webinar training will provide 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 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.

The session will focus 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. We will discuss the classification and valuation of 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.

Areas Covered in the Webinar:

  • The appropriate Multiple Trade Agreements that importers and exporters must be require when conducting trade transactions.
  • 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?

Who Will Benefit:

This online seminar will provide import compliance materials that examine U.S. Customs and Border Protection for international logistics. The target audience includes:

  • 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 regulated products
  • Compliance officers
  • Coordination/Supply chain managers and analysts
  • Trade regulatory/legislative affairs professionals
  • Sales/marketing personnel
  • Training personnel
  • Consultants
  • International business operations
  • Chief Executive Officers
  • Customs or Trade Compliance Personnel or Officers
  • Import or Global Trade Directors or Managers
  • Import Supervisors
Instructor Profile:
Rossano V Gerald

Rossano V Gerald
Academic Professor, Texas A and M University

Dr. Gerald 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; and am also 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. Also, he has developed management and marketing strategies that were used to improve the efficiency and effectiveness of my 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, an MBA in Management from Webster University. Also, study at Thomas Jefferson School of Law where he earned a Master of Science of Law Degree (J.S.M.) for International Taxation and Financial Services in the Risk Compliance & Management field. He also has an MBA in Project Management Degree from the Univ. of Phoenix.

He is 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/ AAPM ® American Academy of Project Management. He also a member of the Council of Supply Chain Management Professionals; and an Advisor for the Mu Kappa Tau Marketing of the Honor Society.

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Refund Policy

Registrants may cancel up to two working days prior to the course start date and will receive a letter of credit to be used towards a future course up to one year from date of issuance. ComplianceOnline would process/provide refund if the Live Webinar has been cancelled. The attendee could choose between the recorded version of the webinar or refund for any cancelled webinar. Refunds will not be given to participants who do not show up for the webinar. On-Demand Recordings can be requested in exchange.

Webinar may be cancelled due to lack of enrolment or unavoidable factors. Registrants will be notified 24hours in advance if a cancellation occurs. Substitutions can happen any time.

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