Reclassification Of The Medicinal Product For Human Use "zemplar" Within The Meaning Of Art. 8, Paragraph 10, Of The Act December 24, 1993, # 537. (Resolution No. 106/2015).

Original Language Title: Riclassificazione del medicinale per uso umano «Zemplar» ai sensidell'art. 8, comma 10, della legge 24 dicembre 1993, n. 537.(Determina n. 106/2015).

Read the untranslated law here:

The DIRECTOR-GENERAL having regard to articles 8 and 9 of legislative decree July 30, 1999, # 300; Visto l'art. September 30, 2003, 48 of Decree-Law n. 269, converted into law November 24, 2003, n. 326, establishing the Italian medicines agency; Having regard to the Decree of the Minister of health in consultation with the Ministers for public administration and Economics and finance dated September 20, 2004, n. 245 laying down rules on the organisation and the functioning of the Italian Medicines Agency, pursuant to paragraph 13 of article. the aforementioned 48 as amended by order No. 53 of the Minister of health, in consultation with the Ministers for public administration and simplification and of economy and Finance of the March 29, 2012; Having regard to the Legislative Decree March 30, 2001, n. 165; Having regard to act July 15, 2002, # 145; Having regard to the Decree of the Minister of health of November 8, 2011, recorded by the Central Office of the budget to the register «Simple» Visas, sheet # 1282, dated November 14, 2011, with which he was appointed Director General of the Italian Medicines Agency. Luca Pani, as from November 16, 2011; Having regard to act December 24, 1993, no. 537 concerning "public finance" corrective action with particular reference to art. 8; Visto l'art. 1, paragraph 40, December 23, 1996, law n. 662 laying «rationalization measures of public finance ", which identifies the margins of distribution for pharmaceutical companies, wholesalers and pharmacists; Visto l'art. 48, paragraph 33, November 24, 2003, law No. 326, which has negotiating the price for products reimbursed by authorisation holders between agency and S. N.; Having regard to the Legislative Decree of April 24, 2006, n. 219, published in the Gazzetta Ufficiale della Repubblica italiana n. 142 of June 21, 2006 on the introduction of Directive 2001/83/EC (and subsequent amending directives) on the Community code relating to medicinal products for human use and Directive 2003/94/EC; Having regard to the Decree-Law no April 28, 2009 39, converted into law June 24, 2009, # 77, with whom art. 13, paragraph 1, point b) is restated the share attributable to drug companies, as provided for in art. 1, section 40 of the Act December 23, 1996, n. 662, 58.65 percent of the retail price exclusive of value added tax; Having regard to the resolution of 1 February 2001 and C.I.P.; View the "notes October 29, 2004 determination AIFA 2004 (Revision Notes CUF) ', published in the ordinary supplement to the official journal # 259 of November 4, 2004 as amended; View the determination A.I.F.A. of July 3, 2006 published in the official journal, General series No 156 of July 7, 2006; View A.I.F.A. determination of September 27, 2006 published in the official journal, General series No. 227, September 29, 2006 concerning "maneuver to the Government subsidized and non-subsidized pharmaceutical shopping»; Given the decree by which the company ABBVIE S.r.l. It was cleared for marketing the medicine "Zemplar" (paracalcitolo); View the determination regarding the classification of the medicinal product in accordance with art. 12, paragraph 5, reads November 8, 2012, # 189; Having regard to the application with which the company ABBVIE S.r.l. has applied for reclassification of the Pack code A.I.C. # 036374130; Having regard to the opinion of the scientific and Technical Advisory Committee of December 10, 2014; Having regard to resolution No. 1 of January 30, 2015 of the Management Board of A.I.F.A. adopted on a proposal from the Director General;
Causes: Art. 1 Classification for the purposes of new listings is the medicine ZEMPLAR (paracalcitolo) in the box below it is classified as follows: package: «5 mcg/ml solution for injection 5 ml glass vials from 1 '-A.I.C. # 036374130 (10) 12Q1ML (based on 32);
New listings ' class: «A»;
Ex factory price (excluding VAT): €101.00;
Price (VAT included): €166.69;
Validity of the contract: 24 months. Discount required to public facilities on the price ' Ex Factory ' as negotiating conditions.