On: September 23, 2024 By: David Noah
Understand the role of the Foreign Principal Party in Interest (FPPI) in export transactions, their responsibilities in routed shipments, and how to ensure compliance when filing through AES.
On: September 16, 2024 By: David Noah
Companies that export software have some additional compliance challenges not faced when exporting physical products, especially if the software is encrypted. These five tips for exporting software will help your company stay compliant.
On: September 4, 2024 By: David Noah
The Shipper’s Letter of Instruction (SLI) is one document that some exporters are reluctant to prepare. They shouldn’t be. An SLI provides a written record of who received the shipping forms, who to contact for questions, who to contact for proof of export, and who verified export compliance.
On: August 26, 2024 By: David Noah
Exporters must be aware of what red flags are, why they matter for export controls and what your responsibilities are under U.S. export regulations.
On: August 19, 2024 By: Lindsay Bernsen Wardlaw
U.S. export controls may apply to your import-only business that never ships goods outside the United States. Design work, software code, prototypes and ideas could all be subject to regulations, even if you never share with people sitting outside the U.S.
On: August 14, 2024 By: Kari Crane
This article explains the expanding U.S. export controls targeting Russia and Belarus, including new license requirements, reduced license exceptions, in-country transfer controls and the latest BIS actions, including additions to the Entity List and Temporary Denial Orders. We share our recommendations for staying up-to-date and compliant.
On: August 7, 2024 By: David Noah
If your company exports goods valued at more than $2,500 to anywhere other than Canada or exports goods that require an export license, U.S. Foreign Trade Regulations require that you file your export information electronically through the Automated Export System (AES). There's an easy way and a hard way...
On: July 31, 2024 By: Kari Crane
Proper product classification is crucial for adhering to export regulations, avoiding delays and preventing costly fines. Unfortunately, many exporters frequently make common errors in this area. We explain the eight most common mistakes and practical tips to help you avoid them.
On: July 29, 2024 By: Kari Crane
Changes in EU Medical Device Regulation have created significant challenges for U.S. exporters, including higher costs and difficulty obtaining certification for products.
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