Review Product Marketing Authorisation For Human Use «Yvidually».

Original Language Title: Modifica dell'autorizzazione all'immissione in commercio delmedicinale per uso umano «Yvidually».

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Retrieved February 24, 2015 V&A # 368/2015 of authorization determines variation in relation to medicine YVIDUALLY are authorized the following variation: insertion of the final study report of the trial 14701 regarding medicinal product and authorisation authorised pack sizes in Italy following the mutual recognition procedure.
How to: NL/H/2041/001/II/006 type of variation: C.I. 4 Mah: Bayer S.p.a.
Inventory disposal lots already products can be kept on the market until the expiration date printed on the label of the medicinal product in accordance with art. 1 subparagraph 5 of determines AIFA n. 371 of 14/04/2014 published in the Official Journal No. 101 of 3/05/2014.
Date of application of determining this determination is effective on the day following that of its publication, to decompress, in Gazzetta Ufficiale della Repubblica italiana and company will be notified to the holder of the marketing authorisation for the medicinal product.