Section 417 of the Food and Drug Modernization Act (FDAMA) of 1997 requires that any company involved in the manufacture, reprocessing, advertising, assembly, or processing of drugs and medical devices that wishes to import them into the United States must do one thing the FDA has to be registered and on the other hand has to show the cooperation with a United States agent.
With MEDAGENT Inc. we provide you with the U.S. Agents aside and thus cover the licensing requirements of the USA. Nothing stands in the way of your approval there!
Contact U.S. Agent
Contact us to find out more about the U.S. MEDAGENT service. Agent’s to find out.