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Webinar - live GST for Non-Resident Importers

Are you a Non-resident importer carrying on business in Canada? Attend this webinar to learn about the Canadian Goods and Services Tax (“GST”) and the Harmonized Sales Tax (“HST”), and how it applies to Non-resident importers. Our experts will provide... Read more >

Webinar - live Incoterms 2010: Is Your Company At Risk?

Are you using the right Incoterm for your business liability and profitability? International Commercial Terms, known as INCOTERMS, help to bring countries with different trading practices together. Defining import and export responsibilities between the buyer and seller are essential to... 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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