Renegotiation Of The Medicinal Product For Human Use "tecfidera (Dimethylfumarate) ' Within The Meaning Of Article 8, Paragraph 10, Of The Act December 24, 1993, # 537. (Resolution No. 7/2015).
Original Language Title: Rinegoziazione del medicinale per uso umano «Tecfidera(dimetilfumarato)» ai sensi dell'articolo 8, comma 10, della legge 24dicembre 1993, n. 537. (Determina n. 7/2015).
Read the untranslated law here: http://www.gazzettaufficiale.it/atto/serie_generale/caricaArticoloDefault/originario?atto.dataPubblicazioneGazzetta=2015-01-24&atto.codiceRedazionale=15A00394&elenco30giorni=false&atto.tipoProvvedimento=DECRETO
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 the Decree-Law September 13, 2012, # 158, converted, with amendments by law November 8, 2012, n. 189 laying down "urgent provisions to promote the development of the country through a higher level of health protection ' and, in particular, article. 12, paragraph 5; 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 1 February 2001 CIPE; 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 AIFA'S determination of July 3, 2006 published in the official journal, General series No 156 of July 7, 2006; View AIFA 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 shopping nearmaceutica '; Given the decree by which the company Biogen and placing the medicinal product has been authorised at «Tecfidera»; Having regard to the determination of 339/2014 April 1, 2014, n. pubblicata nella Gazzetta Ufficiale della Repubblica italiana n. 94 of April 23, 2014, on the classification of the medicinal product in accordance with art. 12, paragraph 5, reads November 8, 2012, n. 189 of medicinal products for human use centrally approved; Having regard to the application with which the firm Biogen has applied for reclassification of A.I.C. code packs # 043217013/E and 043217025 n. A.I.C. (s); Having regard to the opinion of the scientific and Technical Advisory Committee of September 17, 2014; Having regard to the opinion of the pricing and reimbursement at its meeting of November 26, 2014; Having regard to resolution No. 46 of December 16, 2014 AIFA's Board of Directors adopted on the proposal of the Director General;
Causes: Art. 1 Classification for the purposes of new listings is the medicine TECFIDERA (dimethylfumarate) in the packages below and is billed as follows: pack size: 120 mg capsule enteric coated-oral-blister (pvc/pe/pvdc aluminium-pvc)-14 capsules;
A.I.C. # 043217013/E (10) 196W3P (based on 32);
New listings ': class ' A ' Note 65;
Ex factory price (excluding VAT): €144.13;
Price (VAT included): €237.87;
Package: 240 mg enteric coated capsule-oral-blister (pvc/pe/pvdc aluminium-pvc)-56 capsules;
A.I.C. # 043217025/E (10) 196W41 (based on 32);
New listings ': class ' A ' Note 65;
Ex factory price (excluding VAT): €1153.00;
Price (VAT included): €1902.91;
Validity of the contract: 24 months. Discount required to public facilities on the price Ex Factory as per contractual terms.
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