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(V)", "@sens": "cible", "@cidtexte": "JORFTEXT000029676038", "@nortexte": "AFSX1419044D", "@numtexte": "2014-1288", "@typelien": "CITATION", "@naturetexte": "DECRET", "@datesignatexte": "2014-10-23" }, { "@id": "LEGIARTI000048701765", "@num": "L5121-1", "#text": "Code de la santé publique - art. L5121-1 (V)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000041721215", "@num": "L5121-12", "#text": "Code de la santé publique - art. L5121-12 (VD)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000048703410", "@num": "L5121-14-3", "#text": "Code de la santé publique - art. L5121-14-3 (V)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006689889", "@num": "L5121-8", "#text": "Code de la santé publique - art. L5121-8 (M)", "@sens": "source", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006689934", "@num": "L5122-3", "#text": "Code de la santé publique - art. L5122-3 (V)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000044628302", "@num": "L5123-2", "#text": "Code de la santé publique - art. L5123-2 (V)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000048703364", "@num": "L5124-13", "#text": "Code de la santé publique - art. 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Lorsqu'un médicament est autorisé dans un autre Etat membre de la Communauté européenne ou un Etat partie à l'accord sur l'Espace économique européen mais qu'il ne fait l'objet en France ni de l'autorisation de mise sur le marché prévue à l'article L. 5121-8, ni d'une demande en cours d'instruction en vue d'une telle autorisation, l'Agence française de sécurité sanitaire des produits de santé peut, pour des raisons de santé publique justifiées, autoriser la mise sur le marché de ce médicament. L'autorisation peut être délivrée pour une durée déterminée et renouvelée dans des conditions fixées par décret en Conseil d'Etat.
\n
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L'achat, la fourniture, la prise en charge et l'utilisation par les collectivités publiques des médicaments définis aux articles L. 5121-8, L. 5121-9-1, L. 5121-12 et L. 5121-13 ou importés selon la procédure prévue à l'article L. 5124-17-1 sont limités, dans les conditions propres à ces médicaments fixées par le décret mentionné à l'article L. 162-17 du code de la sécurité sociale, aux produits agréés dont la liste est établie par arrêté des ministres chargés de la santé et de la sécurité sociale.
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L'inscription d'un médicament sur la liste mentionnée au premier alinéa peut, au vu des exigences de qualité et de sécurité des soins mettant en oeuvre ce médicament, énoncées le cas échéant par la commission prévue à l'article L. 5123-3, être assortie de conditions concernant la qualification ou la compétence des prescripteurs, l'environnement technique ou l'organisation de ces soins et d'un dispositif de suivi des patients traités.
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L'importation sur le territoire douanier des médicaments à usage humain et l'importation et l'exportation des préparations de thérapie génique ou des préparations de thérapie cellulaire xénogénique mentionnées au 12° et au 13° de l'article L. 5121-1 sont soumises à une autorisation préalable délivrée par l'Agence française de sécurité sanitaire des produits de santé.
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L'autorisation de mise sur le marché prévue à l'article L. 5121-8, l'enregistrement prévu à l'article L. 5121-13 ou l'autorisation prévue au 12° et au 13° de l'article L. 5121-1 valent autorisation au sens de l'alinéa précédent.
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Une telle autorisation n'est pas requise pour le particulier qui transporte personnellement un médicament.
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Lorsqu'un particulier procède à l'importation d'un médicament par une autre voie que le transport personnel, il n'est pas non plus soumis à l'obligation d'une autorisation préalable si ce médicament fait l'objet d'une autorisation de mise sur le marché au sens de l'article 6 de la directive 2001/83/CE du Parlement européen et du Conseil, du 6 novembre 2001, instituant un code communautaire relatif aux médicaments à usage humain ou d'un enregistrement au sens des articles 14 et 16 bis de la même directive dans un Etat membre de la Communauté européenne ou un Etat partie à l'accord sur l'Espace économique européen.
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Le prix de cession au public des spécialités disposant d'une autorisation de mise sur le marché, de l'autorisation mentionnée à l'article L. 5124-17-1 du code de la santé publique ou de l'autorisation mentionnée à l'article L. 5121-9-1 du même code et inscrites sur la liste prévue à l'article L. 5126-4 du code de la santé publique, majoré le cas échéant du montant de la taxe sur la valeur ajoutée, est égal au prix de vente aux établissements de santé déclaré par l'entreprise au Comité économique des produits de santé et publié par ce dernier, auquel s'ajoute une marge dont la valeur est fixée par arrêté des ministres chargés de la santé, de la sécurité sociale et de l'économie prenant en compte les frais inhérents à la gestion et à la dispensation de ces spécialités.
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A défaut de déclaration ou en cas d'opposition définitive du comité, le prix de cession au public est fixé par décision du Comité économique des produits de santé et au plus tard dans un délai de soixante-quinze jours après l'inscription de la spécialité sur la liste prévue à l'article L. 5126-4 du code de la santé publique, ou lorsque la spécialité figurait sur cette liste préalablement à l'obtention de l'autorisation de mise sur le marché, dans un délai de soixante-quinze jours après l'obtention de cette autorisation. Les ministres concernés peuvent faire opposition conjointe à la décision du comité et arrêtent dans ce cas le tarif de responsabilité dans un délai de quinze jours après cette décision. La fixation du prix de cession tient compte principalement des prix de vente pratiqués pour cette spécialité, des prix des médicaments à même visée thérapeutique, des volumes de vente prévus ou constatés, des conditions prévisibles ou réelles d'utilisation du médicament et de l'amélioration du service médical apportée par le médicament appréciée par la commission prévue à l'article L. 5123-3 du même code, ainsi que des frais inhérents à la gestion et à la délivrance de la spécialité pharmaceutique.
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Tant que le prix de vente déclaré ou le prix de cession au public n'est pas publié, les spécialités pharmaceutiques qui figuraient sur cette liste préalablement à l'obtention de l'autorisation de mise sur le marché sont prises en charge ou donnent lieu à remboursement par l'assurance maladie lorsqu'elles sont délivrées par une pharmacie à usage intérieur d'un établissement de santé dûment autorisé sur la base de leur prix d'achat majoré de la marge mentionnée au premier alinéa et, le cas échéant, du montant de la taxe sur la valeur ajoutée.
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Un accord conclu à cet effet entre le comité et une ou plusieurs organisations syndicales représentatives des entreprises concernées ou, à défaut, un décret en Conseil d'Etat précise la procédure, les conditions dans lesquelles sont effectuées les déclarations des laboratoires exploitants, les critères de l'opposition du comité, les conditions dans lesquelles les prix de vente déclarés peuvent être révisés et les engagements que doit prendre l'entreprise.
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Sont constatées et poursuivies dans les conditions fixées par le titre V du livre IV du code de commerce les infractions aux conventions et arrêtés mentionnés ci-dessus.
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Article 58 ENTIEREMENT_MODIF (Loi n° 2006-1640 du 21 décembre 2006 de financement de la sécurité sociale pour 2007 (1))