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

Website https://goo.gl/S5eNLn | Edit Freely

Category FDA Regulated Webinar, fda regulations, fda regulatory affairs training

Deadline: December 14, 2017 | Date: December 14, 2017

Venue/Country: CO, U.S.A

Updated: 2017-11-20 18:31:52 (GMT+9)

Call For Papers - CFP

This webinar 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 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

• 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

• 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

• Logistics/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

LEARNING OBJECTIVES

• 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

For more detail please click on this below link:

https://goo.gl/S5eNLn

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