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Mandatory labeling procedure for drug products
Federal Act no. 425-FZ from 28 December 2017 modifies provisions of Drug Products Circulation Act. It abides participants of civil circulation to label drug products with secific means of identification, as well as file regular reports via system of Drug Products Circulation covering all operations involving labeled drug products.
Requirements for mandatory drug product labeling and communicating all the information on the drug products to the labeling systemcomes into effect from 1 July 2020.