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Validity : 17th Sep'26 to 27th Sep'26
60 Mins
Basic & Intermediate & Advanced
This training event provided guidance on how to access FDA agency documentation that is 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 agricultural commodities and Food, Drugs and Cosmetics that may be marked as adulterated, mislabeled or misbranded by using procedural and cases.
It 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 FDA guidelines by U.S. Port of Entry requirements developed and developing markets. This review FDA procedures and evaluation criterion will influence the coordination 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.