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The Bill (Reg.№2625) introduces the amendments to the Article 12 of the current Law according to which there should be indicated on the external package of the medicines with the Braille the name of the medicines, dose of the active substance and medical form.

The suggested norm of the bill correspond to the European System of Laws, firs of all to the Article 56 (a) of the Directive 2001/83/EU

 

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