Title 21 › CHAPTER 9 — FEDERAL FOOD, DRUG, AND COSMETIC ACT › SUBCHAPTER V — DRUGS AND DEVICES › Part H — Pharmaceutical Distribution Supply Chain › § 360eee–3
Third-party logistics providers must have every facility they use be licensed. Each facility must be licensed by the State where the drug is sent from. If that State has no license program, the Secretary must issue the license. If the provider ships drugs across State lines, the facility must also be licensed by the State receiving the drug when that State requires it and the provider is not licensed by the Secretary. Starting 1 year after November 27, 2013, each facility must report once a year to the Secretary the State that issued the license and the license number, plus the facility’s name, address, and any trade names. If a State has no license program, the Secretary may charge a fee to cover the cost of licensing and inspections, subject to appropriations; States with programs may charge fees, and States without programs may not. By 2 years after November 27, 2013, the Secretary must write rules covering licensing, inspections, storage and security practices (including recordkeeping, recalls, quarantines, and emergency plans), background checks, bans on managers convicted of certain felonies, accreditation and licensing processes, and 3-year license terms with renewals. The rulemaking must allow at least 60 days for comment and the final rules take effect 1 year after they are issued.
Full Legal Text
Food and Drugs, Source: USLM XML via OLRC
Reference
Citation
21 U.S.C. § 360eee–3
Title 21, Food and Drugs
Last Updated
Sep 22, 2026
Release point: 119-110