Avrupa Birliği tıbbi ürünlerin gönderimi konusunda yeni direktif. (İng)
EU Publishes new Delegated Act on Shipments of Medicinal Products through EU
Directive 2011/62/EU, the Falsified Medicines Directive requires Member States to prevent medicinal products that are introduced into the EU, but are not intended to be placed on the EU market, from entering into circulation if there are sufficient grounds to suspect that those products are falsified. Member states have to implement this requirement from 2 January 2013.