Assistance with U.S. FDA Regulations
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Radiation-Emitting
Devices
Every manufacturer of electronic products, prior to offering such product for importation into the United States, must designate a U.S. Agent for service of processes. In addition, some manufacturers, assemblers, or importers may be required to provide additional Product Reports to FDA.
Tobacco products marketed in the United States are regulated by the U.S. Food and Drug Administration (FDA). FDA’s authority extends to all tobacco products, including (but not limited to) e-cigarettes, cigars, hookah tobacco, pipe tobacco, and roll your own (RYO) tobacco.
Tobacco
Biologics
Registrar Corp assists with FDA requirements for Biologics, including Blood Establishment Registration and registration and listing for Human Cells, Tissues, and Cellular and Tissue-Based Products (HCT/P’s).
