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Webinar - live The Basics: U.S. Customs Valuation

In light of the duties recently imposed on certain goods by the U.S. government, valuation has become an important process for importers. Businesses that understand the valuation process and have eligible goods, can significantly minimize unexpected duty outlays. Reasonable care... Read more >

Webinar - live An introduction to CPTPP

The Comprehensive and Progressive Agreement for Trans-Pacific Partnership (CPTPP) is a free trade agreement between Canada and 10 other countries in the Asia-Pacific region: Australia, Brunei, Chile, Japan, Malaysia, Mexico, New Zealand, Peru, Singapore and Vietnam. Once fully implemented, these... Read more >

Article FDA registration renewal – does it apply to you?

The food facility update period starts on October 1st RENEW YOUR FDA REGISTRATION TODAY. Under the Food and Safety Modernization Act (FSMA), the Food and Drug Administration (FDA) requires domestic and foreign facilities that manufacture, pack, or hold food for... Read more >

Best practices FDA Data Elements

This guide was put together as an additional resource, aside from the UPKs, including each FDA Program group, to address areas within FDA that now require decision making based upon the product you have as to what will be required... Read more >

Best practices FDA Intended Use

Importing FDA-regulated products? As a customs broker, Livingston needs to know how the product being imported is intended to be used and/or why the product is being imported. Importers should confirm that their invoices clearly show what the end use... Read more >

Best practices FDA Affirmations of Compliance

Affirmations of compliance are additional pieces of information such as medical device listing, drug listing, Radiation Declaration, FCE/SIDS (canning establishment). In all, there are more than 200 different types of Affirmations of Compliance in the differing industries within FDA jurisdiction.... Read more >

Best practices FDA Government Agency Processing Codes

Many products will need these government agency processing codes as a way to tell the FDA more about what type of product category this item is in. As some of these codes can be determined by the customs broker, it’s... Read more >

Webinar - on demand FDA Compliance Under ACE

The U.S. Food and Drug Administration (FDA) requires the electronic transmission of data elements such as FDA product code; description; country of production; cargo storage status; manufacturer ID; and Shipper ID. With ACE in effect, FDA data will no longer... Read more >

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