To the attention of interested persons
For medicinal products authorised through national/decentralised/ mutual recognition procedure, prior to entering into force of rules for classification for release, approved through Order of the Minister of Health No. 1602/2010, until renewal of authorisation or within one year from the entering into force of these Rules (for medicinal products with permanent authorisation), the wording used for classification subcategories will be assimilated to the wording adopted through these Rules, in accordance with the attached document.
As regards medicinal products authorised through centralised procedure, the wording employed for the subcategories for classification for release will be assimilated to the wording adopted through Scientific Council Decision No. 13/2010 (harmonising the classification for release of medicinal products authorised through centralised procedure with the one used for other types of procedures), in accordance with the attached document.
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