Manufacturers & Providers
MoH: Announcement of round table, organized to inform Romanian Manufacturers and Marketing Authorization Holders about the steps to be taken to meet the requirements of European Directive 2011/62, also known as the "Falsified Medicines Directive".
At this round table will be presented the stage of implementation of the EC Directive 2011/62 in Romania as well as the procedure that the Romanian drug manufacturers will have to apply in order to be able to enter the testing phase of the connection with the European database. The procedure will be presented by an expert of the European Medicines Control Organization, who will be able to answer this opportunity and the questions of the participants. Participation in this event is free of charge, subject to registration until October 3, 2017, at the following e-mail address: email@example.com.
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