Review Product Marketing Authorisation For Human Use «Sonirem».

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

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Retrieved February 24, 2015 V&A # 364/2015 determines the (authorization of changes concerning the medicine SONIREM) are authorized the following variation: approval of the Risk management Plan of Sonirem with its post-approval commitments concerning the medicinal product and authorisation authorised pack sizes in Italy following the mutual recognition procedure.
How to: en/H/0187/001/II/008 type of variation: c. I z) Mah: ITALFARMACO S.P. stock 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 Gazette No. 101 of 03/05/2014.
Date of determination: 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.