An In Vitro Diagnostic Import License is a regulatory authorization granted by government health agencies to entities involved in the importation of in vitro diagnostic (IVD) products. These licenses are essential for ensuring that imported diagnostic devices comply with quality and safety standards, as well as adhere to the regulatory requirements of the destination country. The license is a crucial component in the global healthcare supply chain, as it helps maintain the integrity of diagnostic testing procedures by monitoring and controlling the entry of IVD products into a particular market.
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