USFDA And CBP Bolster Collaboration To Protect Public Health And Safety

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On April 04, 2019, an agreement was signed between the USFDA and the U.S. Customs and Border Protection leaders to maximize inspection and detection capabilities in order to prevent illegal and harmful products, ...
United States Food, Drugs, Healthcare, Life Sciences

On April 04, 2019, an agreement was signed between the U.S. Food and Drug Administration and the U.S. Customs and Border Protection (CBP) leaders to maximize inspection and detection capabilities in order to prevent illegal and harmful products, that pose a threat to public health, from entering the U.S. through the nation's International

Mail Facilities (IMFs) and Ports of Entry1. This agreement enables each agency to work towards: Enhancing knowledge-transfer to increase efficiency, reduce duplication of efforts and facilitate mission responsibilities.

  • Collaboration on shared laboratory space, scientific equipment and facilities, along with intellectual, historical and institutional knowledge will optimize the resources at each agency's disposal.

In 2018, FDA staff posted at the IMFs around the country examined packages from more than 180 countries. Approximately 90 percent of the packages reviewed by the FDA contained products that should not have been entering the country. Most mail arrives in an IMF without advanced or specific identifying information. The FDA uses advanced screening technology to assess the contents of these packages and to increase efficiency of the agency's overall investigational capabilities.

The FDA and CBP with this agreement will expand how information is shared between the agencies to identify trends which can target future entries. This may include general data points on frequent countries of origin, as well as specific products and volumes of packages at each location.

An additional focus of this effort will be coordinating shared space as well as increased scientific presence at high-risk/high-volume IMF locations, helping to facilitate and support real-time entry decisions and increased data sharing. Additionally, the FDA and CBP will enhance coordination around efforts to identify violative packages and develop new targeting and enforcement strategies at Ports of Entry.

Note- At present, there are nine IMF locations across the U.S., with one location each in Florida, Hawaii, Illinois, New Jersey, New York, Puerto Rico, U.S. Virgin Islands respectively and two locations in California. CBP provides security and facilitation operations at 328 Ports of Entry throughout the country.

Footnote

1. https://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/ucm635270.htm

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