{ "article": { "LEGIARTI000006694300": { "META": { "META_SPEC": { "META_ARTICLE": { "NUM": "L670-5", "ETAT": "ABROGE", "TYPE": "AUTONOME", "DATE_FIN": "2000-06-22", "DATE_DEBUT": "1994-07-30" } }, "META_COMMUN": { "ID": "LEGIARTI000006694300", "URL": "article/LEGI/ARTI/00/00/06/69/43/LEGIARTI000006694300.xml", "NATURE": "Article", "ORIGINE": "LEGI", "ANCIEN_ID": "SPAOXXXXXXX1X670L05AXXAB" } }, "LIENS": { "LIEN": [ { "@id": "JORFTEXT000000503843", "#text": "Décret 53-1001 1953-10-05 (décret de codification)", "@sens": "source", "@cidtexte": "JORFTEXT000000503843", "@numtexte": "53-1001", "@typelien": "CODIFICATION", "@naturetexte": "DECRET", "@datesignatexte": "1953-10-05" }, { "@id": "LEGITEXT000005615433", "#text": "Décret n°94-193 du 7 mars 1994", "@sens": "cible", "@cidtexte": "JORFTEXT000000364005", "@nortexte": "SPSP9400453D", "@numtexte": "94-193", "@typelien": "TXT_SOURCE", "@naturetexte": "DECRET", "@datesignatexte": "1994-03-07" }, { "@id": "LEGIARTI000006698729", "@num": "1", "#text": "Décret n°94-193 du 7 mars 1994 - art. 1 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000000364005", "@nortexte": "SPSP9400453D", "@numtexte": "94-193", "@typelien": "TXT_SOURCE", "@naturetexte": "DECRET", "@datesignatexte": "1994-03-07" }, { "@id": "LEGIARTI000006698730", "@num": "2", "#text": "Décret n°94-193 du 7 mars 1994 - art. 2 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000000364005", "@nortexte": "SPSP9400453D", "@numtexte": "94-193", "@typelien": "TXT_SOURCE", "@naturetexte": "DECRET", "@datesignatexte": "1994-03-07" }, { "@id": "LEGIARTI000006698731", "@num": "3", "#text": "Décret n°94-193 du 7 mars 1994 - art. 3 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000000364005", "@nortexte": "SPSP9400453D", "@numtexte": "94-193", "@typelien": "TXT_SOURCE", "@naturetexte": "DECRET", "@datesignatexte": "1994-03-07" }, { "@id": "LEGIARTI000006698732", "@num": "4", "#text": "Décret n°94-193 du 7 mars 1994 - art. 4 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000000364005", "@nortexte": "SPSP9400453D", "@numtexte": "94-193", "@typelien": "TXT_SOURCE", "@naturetexte": "DECRET", "@datesignatexte": "1994-03-07" }, { "@id": "LEGIARTI000006698733", "@num": "5", "#text": "Décret n°94-193 du 7 mars 1994 - art. 5 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000000364005", "@nortexte": "SPSP9400453D", "@numtexte": "94-193", "@typelien": "TXT_SOURCE", "@naturetexte": "DECRET", "@datesignatexte": "1994-03-07" }, { "@id": "LEGIARTI000006698734", "@num": "6", "#text": "Décret n°94-193 du 7 mars 1994 - art. 6 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000000364005", "@nortexte": "SPSP9400453D", "@numtexte": "94-193", "@typelien": "TXT_SOURCE", "@naturetexte": "DECRET", "@datesignatexte": "1994-03-07" }, { "@id": "LEGIARTI000006698735", "@num": "7", "#text": "Décret n°94-193 du 7 mars 1994 - art. 7 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000000364005", "@nortexte": "SPSP9400453D", "@numtexte": "94-193", "@typelien": "TXT_SOURCE", "@naturetexte": "DECRET", "@datesignatexte": "1994-03-07" }, { "@id": "LEGIARTI000006698736", "@num": "8", "#text": "Décret n°94-193 du 7 mars 1994 - art. 8 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000000364005", "@nortexte": "SPSP9400453D", "@numtexte": "94-193", "@typelien": "TXT_SOURCE", "@naturetexte": "DECRET", "@datesignatexte": "1994-03-07" }, { "@id": "LEGIARTI000006698738", "@num": "9", "#text": "Décret n°94-193 du 7 mars 1994 - art. 9 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000000364005", "@nortexte": "SPSP9400453D", "@numtexte": "94-193", "@typelien": "TXT_SOURCE", "@naturetexte": "DECRET", "@datesignatexte": "1994-03-07" }, { "@id": "LEGIARTI000006696772", "@num": "1", "#text": "Loi n°94-654 du 29 juillet 1994 - art. 1 () JORF 30 juillet 1994", "@sens": "source", "@cidtexte": "JORFTEXT000000549618", "@nortexte": "SPSX9400032L", "@numtexte": "94-654", "@typelien": "MODIFICATION", "@naturetexte": "LOI", "@datesignatexte": "1994-07-29" }, { "@id": "LEGIARTI000006696774", "@num": "3", "#text": "Loi n°94-654 du 29 juillet 1994 - art. 3 () JORF 30 juillet 1994", "@sens": "source", "@cidtexte": "JORFTEXT000000549618", "@nortexte": "SPSX9400032L", "@numtexte": "94-654", "@typelien": "MODIFICATION", "@naturetexte": "LOI", "@datesignatexte": "1994-07-29" }, { "@id": "LEGIARTI000006722899", "@num": "13", "#text": "Décret n°98-79 du 11 février 1998 - art. 13 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000000372654", "@nortexte": "MESP9820016D", "@numtexte": "98-79", "@typelien": "CITATION", "@naturetexte": "DECRET", "@datesignatexte": "1998-02-11" }, { "@id": "JORFTEXT000000217229", "#text": "Ordonnance 2000-548 2000-06-15 art. 4 I JORF 22 juin 2000", "@sens": "source", "@cidtexte": "JORFTEXT000000217229", "@nortexte": "MESX0000036R", "@typelien": "ABROGATION", "@naturetexte": "RAPPORT", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006690011", "@num": "L5124-18", "#text": "Code de la santé publique - art. L5124-18 (M)", "@sens": "source", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CONCORDE", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006690011", "@num": "L5124-18", "#text": "Code de la santé publique - art. L5124-18 (M)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CONCORDANCE", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006694295", "@num": "L670-3", "#text": "Code de la santé publique - art. L670-3 (M)", "@sens": "source", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "#text": "Loi 58-356 1958-04-03 (loi de validation)", "@sens": "source", "@typelien": "CODIFICATION" } ] }, "CONTEXTE": { "TEXTE": { "TM": { "TM": { "TM": { "TM": { "TITRE_TM": [ { "@id": "LEGISCTA000006155377", "@fin": "2000-06-22", "#text": "Chapitre 5 : Des médicaments dérivés du sang et du Laboratoire français du fractionnement et des biotechnologies", "@debut": "1994-07-30" } ] }, "TITRE_TM": [ { "@id": "LEGISCTA000006140791", "@fin": "2000-06-22", "#text": "Titre 2 : Du sang humain", "@debut": "1994-07-30" } ] }, "TITRE_TM": [ { "@id": "LEGISCTA000006125383", "@fin": "2000-06-22", "#text": "Livre 6 : Don et utilisation des éléments et produits du corps humain", "@debut": "1994-07-30" } ] }, "TITRE_TM": [ { "@id": "LEGISCTA000006103420", "@fin": "2999-01-01", "#text": "Partie législative ancienne", "@debut": "1953-10-07" } ] }, "@cid": "LEGITEXT000006072665", "@nature": "CODE", "TITRE_TXT": [ { "@fin": "2999-01-01", "#text": "Code de la santé publique", "@debut": "1953-10-07", "@id_txt": "LEGITEXT000006072665", "@c_titre_court": "Code de la santé publique" } ], "@date_publi": "2999-01-01", "@date_signature": "2999-01-01" } }, "VERSIONS": { "VERSION": [ { "@etat": "MODIFIE", "LIEN_ART": { "@id": "LEGIARTI000006694299", "@fin": "1994-07-30", "@num": "L670-5", "@etat": "MODIFIE", "@debut": "1993-01-05", "@origine": "LEGI" } }, { "@etat": "ABROGE", "LIEN_ART": { "@id": "LEGIARTI000006694300", "@fin": "2000-06-22", "@num": "L670-5", "@etat": "ABROGE", "@debut": "1994-07-30", "@origine": "LEGI" } } ] }, "BLOC_TEXTUEL": { "CONTENU": "
Un décret en Conseil d'Etat fixe, en tant que de besoin, les conditions d'application du présent chapitre. Il précise les sections de l'ordre auxquelles appartiennent les pharmaciens mentionnés à l'article L. 670-3. Il définit les conditions dans lesquelles lesdits pharmaciens doivent être assistés ou remplacés.
\n
" } }, "LEGIARTI000006690011": { "META": { "META_SPEC": { "META_ARTICLE": { "NUM": "L5124-18", "ETAT": "MODIFIE", "TYPE": "AUTONOME", "DATE_FIN": "2002-01-18", "DATE_DEBUT": "2000-06-22" } }, "META_COMMUN": { "ID": "LEGIARTI000006690011", "URL": "article/LEGI/ARTI/00/00/06/69/00/LEGIARTI000006690011.xml", "NATURE": "Article", "ORIGINE": "LEGI", "ANCIEN_ID": "SPANXXXXXXX1X5124L18XXAA" } }, "LIENS": { "LIEN": [ { "@id": "JORFTEXT000000178408", "#text": "Loi 92-1279 1992-12-08 art. 26", "@sens": "source", "@cidtexte": "JORFTEXT000000178408", "@nortexte": "SANX9100161L", "@numtexte": "92-1279", "@typelien": "CONCORDANCE", "@naturetexte": "LOI", "@datesignatexte": "1992-12-08" }, { "@id": "LEGIARTI000006696612", "@num": "26", "#text": "Loi n°92-1279 du 8 décembre 1992 - art. 26 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000000178408", "@nortexte": "SANX9100161L", "@numtexte": "92-1279", "@typelien": "CONCORDE", "@naturetexte": "LOI", "@datesignatexte": "1992-12-08" }, { "@id": "JORFTEXT000000217229", "#text": "Ordonnance 2000-548 2000-06-15", "@sens": "source", "@cidtexte": "JORFTEXT000000217229", "@nortexte": "MESX0000036P", "@typelien": "CODIFICATION", "@naturetexte": "RAPPORT", "@datesignatexte": "2999-01-01" }, { "@id": "JORFTEXT000000227015", "#text": "Loi 2002-303 2002-03-04 art. 92 JORF 5 mars 2002", "@sens": "source", "@cidtexte": "JORFTEXT000000227015", "@nortexte": "MESX0100092L", "@numtexte": "2002-303", "@typelien": "CODIFICATION", "@naturetexte": "LOI", "@datesignatexte": "2002-03-04" }, { "@id": "LEGIARTI000006232083", "@num": "1", "#text": "Décret n°2004-652 du 2 juillet 2004 - art. 1 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000000436351", "@nortexte": "SANG0421847D", "@numtexte": "2004-652", "@typelien": "CITATION", "@naturetexte": "DECRET", "@datesignatexte": "2004-07-02" }, { "@id": "LEGIARTI000006915045", "@num": "D5124-57", "#text": "Code de la santé publique - art. D5124-57 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006915046", "@num": "D5124-57-1", "#text": "Code de la santé publique - art. D5124-57-1 (M)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000036511334", "@num": "L1222-1-1", "#text": "Code de la santé publique - art. L1222-1-1 (V)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000048703397", "@num": "L5121-16", "#text": "Code de la santé publique - art. L5121-16 (V)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000025124663", "@num": "L5121-17", "#text": "Code de la santé publique - art. L5121-17 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006689992", "@num": "L5124-11", "#text": "Code de la santé publique - art. L5124-11 (M)", "@sens": "source", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006689996", "@num": "L5124-13", "#text": "Code de la santé publique - art. 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Sont déterminées par décret en Conseil d'Etat :
\n
1° Les conditions dans lesquelles toute entreprise comportant au moins un établissement pharmaceutique doit être la propriété d'un pharmacien ou d'une société à la gérance ou à la direction de laquelle participe un pharmacien ;
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2° Les modalités d'exercice de la location-gérance prévue au premier alinéa de l'article L. 5124-2 ;
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3° La durée et le contenu de l'expérience pratique appropriée dont doivent justifier les pharmaciens responsables et les pharmaciens délégués, selon les dispositions du dernier alinéa de l'article L. 5124-2 ;
\n
4° Les modalités d'octroi, de suspension ou de retrait de l'autorisation d'ouverture d'un établissement pharmaceutique prévue à l'article L. 5124-3 ;
\n
5° Les conditions dans lesquelles les établissements publics de santé fabriquant industriellement des médicaments au 31 décembre 1991, peuvent demander à bénéficier de l'autorisation prévue à l'article L. 5124-3 ;
\n
6° Les conditions de remplacement prévu à l'article L. 5124-4 des pharmaciens responsables et des pharmaciens délégués en cas d'absence du titulaire ou s'ils font l'objet d'une interdiction d'exercer ;
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7° Les conditions de la gérance d'un établissement pharmaceutique prévue à l'article L. 5124-4 en cas de décès du pharmacien propriétaire ;
\n
8° Les conditions dans lesquelles peut être faite la publicité en faveur des entreprises et établissements pharmaceutiques ;
\n
9° Les modalités d'application des articles L. 5124-7 et L. 5124-8 et les adaptations qui pourront être apportées, en ce qui concerne les établissements pharmaceutiques, aux second, troisième, et quatrième alinéas de l'article L. 5124-2 ;
\n
10° Les conditions dans lesquelles peut être faite la publicité en faveur des établissements pharmaceutiques ;
\n
11° Les règles régissant l'exportation des médicaments prévue à l'article L. 5124-11 ;
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12° Les conditions dans lesquelles l'Agence française de sécurité sanitaire des produits de santé autorise l'importation des médicaments prévue à l'article L. 5124-13 ;
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13° Les sections de l'ordre auxquelles appartient le pharmacien mentionné à l'article L. 5124-15 et les conditions dans lesquelles ce pharmacien doit être assisté ou remplacé.
" } }, "LEGIARTI000006690012": { "META": { "META_SPEC": { "META_ARTICLE": { "NUM": "L5124-18", "ETAT": "MODIFIE", "TYPE": "AUTONOME", "DATE_FIN": "2005-07-29", "DATE_DEBUT": "2002-01-18" } }, "META_COMMUN": { "ID": "LEGIARTI000006690012", "URL": "article/LEGI/ARTI/00/00/06/69/00/LEGIARTI000006690012.xml", "NATURE": "Article", "ORIGINE": "LEGI", "ANCIEN_ID": "SPANXXXXXXX1X5124L18XXAB" } }, "NOTA": { "CONTENU": "
Nota : Loi 2002-73 2002-01-17 art. 12 IV : Les dispositions du présent article entrent en vigueur à la date de publication de l'arrêté nommant les membres du conseil d'administration du Laboratoire français du fractionnement et des biotechnologies.
\n
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Sont déterminés par décret en Conseil d'Etat :
\n
1° Les conditions dans lesquelles toute entreprise comportant au moins un établissement pharmaceutique doit être la propriété d'un pharmacien ou d'une société à la gérance ou à la direction de laquelle participe un pharmacien ;
\n
2° Les modalités d'exercice de la location-gérance prévue au premier alinéa de l'article L. 5124-2 ;
\n
3° La durée et le contenu de l'expérience pratique appropriée dont doivent justifier les pharmaciens responsables et les pharmaciens délégués, selon les dispositions du dernier alinéa de l'article L. 5124-2 ;
\n
4° Les modalités d'octroi, de suspension ou de retrait de l'autorisation d'ouverture d'un établissement pharmaceutique prévue à l'article L. 5124-3 ;
\n
5° Les conditions dans lesquelles les établissements publics de santé fabriquant industriellement des médicaments au 31 décembre 1991, peuvent demander à bénéficier de l'autorisation prévue à l'article L. 5124-3 ;
\n
6° Les conditions de remplacement prévu à l'article L. 5124-4 des pharmaciens responsables et des pharmaciens délégués en cas d'absence du titulaire ou s'ils font l'objet d'une interdiction d'exercer ;
\n
7° Les conditions de la gérance d'un établissement pharmaceutique prévue à l'article L. 5124-4 en cas de décès du pharmacien propriétaire ;
\n
8° Les conditions dans lesquelles peut être faite la publicité en faveur des entreprises et établissements pharmaceutiques ;
\n
9° Les modalités d'application des articles L. 5124-7 et L. 5124-8 et les adaptations qui pourront être apportées, en ce qui concerne les établissements pharmaceutiques, aux second, troisième, et quatrième alinéas de l'article L. 5124-2 ;
\n
10° Les conditions dans lesquelles peut être faite la publicité en faveur des établissements pharmaceutiques ;
\n
11° Les règles régissant l'exportation des médicaments prévue à l'article L. 5124-11 ;
\n
12° Les conditions dans lesquelles l'Agence française de sécurité sanitaire des produits de santé autorise l'importation des médicaments prévue à l'article L. 5124-13 ;
\n
13° Les sections de l'ordre auxquelles appartient le pharmacien mentionné à l'article L. 5124-15 et les conditions dans lesquelles ce pharmacien doit être assisté ou remplacé ;
\n
14° Le statut du Laboratoire français du fractionnement et des biotechnologies.
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Sont déterminés par décret en Conseil d'Etat :
\n
1° Les conditions dans lesquelles toute entreprise comportant au moins un établissement pharmaceutique doit être la propriété d'un pharmacien ou d'une société à la gérance ou à la direction de laquelle participe un pharmacien ;
\n
2° Les modalités d'exercice de la location-gérance prévue au premier alinéa de l'article L. 5124-2 ;
\n
3° La durée et le contenu de l'expérience pratique appropriée dont doivent justifier les pharmaciens responsables et les pharmaciens délégués, selon les dispositions du dernier alinéa de l'article L. 5124-2 ;
\n
4° Les modalités d'octroi, de suspension ou de retrait de l'autorisation d'ouverture d'un établissement pharmaceutique prévue à l'article L. 5124-3 ;
\n
5° Les conditions dans lesquelles les établissements publics de santé fabriquant industriellement des médicaments au 31 décembre 1991, peuvent demander à bénéficier de l'autorisation prévue à l'article L. 5124-3 ;
\n
6° Les conditions de remplacement prévu à l'article L. 5124-4 des pharmaciens responsables et des pharmaciens délégués en cas d'absence du titulaire ou s'ils font l'objet d'une interdiction d'exercer ;
\n
7° Les conditions de la gérance d'un établissement pharmaceutique prévue à l'article L. 5124-4 en cas de décès du pharmacien propriétaire ;
\n
8° Les conditions dans lesquelles peut être faite la publicité en faveur des entreprises et établissements pharmaceutiques ;
\n
9° Les modalités d'application des articles L. 5124-7 et L. 5124-8 et les adaptations qui pourront être apportées, en ce qui concerne les établissements pharmaceutiques, aux second, troisième, et quatrième alinéas de l'article L. 5124-2 ;
\n
10° Les conditions dans lesquelles peut être faite la publicité en faveur des établissements pharmaceutiques ;
\n
11° Les règles régissant l'exportation des médicaments prévue à l'article L. 5124-11 ;
\n
12° Les conditions dans lesquelles l'Agence française de sécurité sanitaire des produits de santé autorise l'importation des médicaments prévue à l'article L. 5124-13 ;
\n
13° Les sections de l'ordre auxquelles appartient le pharmacien mentionné à l'article L. 5124-15 et les conditions dans lesquelles ce pharmacien doit être assisté ou remplacé.
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L245-1 (V)", "@sens": "cible", "@cidtexte": "LEGITEXT000006073189", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" } ] }, "CONTEXTE": { "TEXTE": { "TM": { "TM": { "TM": { "TM": { "TM": { "TITRE_TM": [ { "@id": "LEGISCTA000006171369", "@fin": "2999-01-01", "#text": "Chapitre IV : Fabrication et distribution en gros.", "@debut": "2000-06-22" } ] }, "TITRE_TM": [ { "@id": "LEGISCTA000006155085", "@fin": "2999-01-01", "#text": "Titre II : Médicaments à usage humain", "@debut": "2000-06-22" } ] }, "TITRE_TM": [ { "@id": "LEGISCTA000006140630", "@fin": "2999-01-01", "#text": "Livre Ier : Produits pharmaceutiques", "@debut": "2000-06-22" } ] }, "TITRE_TM": [ { "@id": "LEGISCTA000006125349", "@fin": "2999-01-01", "#text": "Cinquième partie : Produits de santé", "@debut": "2000-06-22" } ] }, "TITRE_TM": [ { "@id": "LEGISCTA000006103419", "@fin": "2999-01-01", "#text": "Partie législative", "@debut": "2000-06-22" } ] }, "@cid": "LEGITEXT000006072665", "@nature": "CODE", "TITRE_TXT": [ { "@fin": "2999-01-01", "#text": "Code de la santé publique", "@debut": "1953-10-07", "@id_txt": "LEGITEXT000006072665", "@c_titre_court": "Code de la santé publique" } ], "@date_publi": "2999-01-01", "@date_signature": "2999-01-01" } }, "VERSIONS": { "VERSION": [ { "@etat": "MODIFIE", "LIEN_ART": { "@id": "LEGIARTI000006690011", "@fin": "2002-01-18", "@num": "L5124-18", "@etat": "MODIFIE", "@debut": "2000-06-22", "@origine": "LEGI" } }, { "@etat": "MODIFIE", "LIEN_ART": { "@id": "LEGIARTI000006690012", "@fin": "2005-07-29", "@num": "L5124-18", "@etat": "MODIFIE", "@debut": "2002-01-18", "@origine": "LEGI" } }, { "@etat": "MODIFIE", "LIEN_ART": { "@id": "LEGIARTI000006690013", "@fin": "2007-03-06", "@num": "L5124-18", "@etat": "MODIFIE", "@debut": "2005-07-29", "@origine": "LEGI" } }, { "@etat": "MODIFIE", "LIEN_ART": { "@id": "LEGIARTI000006690014", "@fin": "2011-03-24", "@num": "L5124-18", "@etat": "MODIFIE", "@debut": "2007-03-06", "@origine": "LEGI" } }, { "@etat": "MODIFIE", "LIEN_ART": { "@id": "LEGIARTI000023755067", "@fin": "2012-05-01", "@num": "L5124-18", "@etat": "MODIFIE", "@debut": "2011-03-24", "@origine": "LEGI" } }, { "@etat": "MODIFIE", "LIEN_ART": { "@id": "LEGIARTI000025104409", "@fin": "2016-05-01", "@num": "L5124-18", "@etat": "MODIFIE", "@debut": "2012-05-01", "@origine": "LEGI" } }, { "@etat": "MODIFIE", "LIEN_ART": { "@id": "LEGIARTI000032411571", "@fin": "2019-12-28", "@num": "L5124-18", "@etat": "MODIFIE", "@debut": "2016-05-01", "@origine": "LEGI" } }, { "@etat": "MODIFIE", "LIEN_ART": { "@id": "LEGIARTI000041397437", "@fin": "2023-12-28", "@num": "L5124-18", "@etat": "MODIFIE", "@debut": "2019-12-28", "@origine": "LEGI" } }, { "@etat": "VIGUEUR", "LIEN_ART": { "@id": "LEGIARTI000048703322", "@fin": "2999-01-01", "@num": "L5124-18", "@etat": "VIGUEUR", "@debut": "2023-12-28", "@origine": "LEGI" } } ] }, "BLOC_TEXTUEL": { "CONTENU": "
Sont déterminés par décret en Conseil d'Etat :
\n
1° Les conditions dans lesquelles toute entreprise comportant au moins un établissement pharmaceutique doit être la propriété d'un pharmacien ou d'une société à la gérance ou à la direction de laquelle participe un pharmacien ;
\n
2° Les modalités d'exercice de la location-gérance prévue au premier alinéa de l'article L. 5124-2 ;
\n
3° La durée et le contenu de l'expérience pratique appropriée dont doivent justifier les pharmaciens responsables et les pharmaciens délégués, selon les dispositions du dernier alinéa de l'article L. 5124-2 ;
\n
4° Les modalités d'octroi, de suspension ou de retrait de l'autorisation d'ouverture d'un établissement pharmaceutique prévue à l'article L. 5124-3 ;
\n
5° Les conditions dans lesquelles les établissements publics de santé fabriquant industriellement des médicaments au 31 décembre 1991, peuvent demander à bénéficier de l'autorisation prévue à l'article L. 5124-3 ;
\n
6° Les conditions de remplacement prévu à l'article L. 5124-4 des pharmaciens responsables et des pharmaciens délégués en cas d'absence du titulaire ou s'ils font l'objet d'une interdiction d'exercer ;
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7° Les conditions de la gérance d'un établissement pharmaceutique prévue à l'article L. 5124-4 en cas de décès du pharmacien propriétaire ;
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8° Les conditions dans lesquelles peut être faite la publicité en faveur des entreprises et établissements pharmaceutiques ;
\n
9° Les modalités d'application des articles L. 3135-1, L. 5124-7 et L. 5124-8 et les adaptations qui pourront être apportées, en ce qui concerne les établissements pharmaceutiques, aux second, troisième, et quatrième alinéas de l'article L. 5124-2 ;
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10° Les conditions dans lesquelles peut être faite la publicité en faveur des établissements pharmaceutiques ;
\n
11° Les règles régissant l'exportation des médicaments prévue à l'article L. 5124-11 ;
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12° Les conditions dans lesquelles l'Agence française de sécurité sanitaire des produits de santé autorise l'importation des médicaments prévue à l'article L. 5124-13 ;
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13° Les sections de l'ordre auxquelles appartient le pharmacien mentionné à l'article L. 5124-15 et les conditions dans lesquelles ce pharmacien doit être assisté ou remplacé.
" } }, "LEGIARTI000006694295": { "META": { "META_SPEC": { "META_ARTICLE": { "NUM": "L670-3", "ETAT": "MODIFIE", "TYPE": "AUTONOME", "DATE_FIN": "1994-07-30", "DATE_DEBUT": "1993-01-05" } }, "META_COMMUN": { "ID": "LEGIARTI000006694295", "URL": "article/LEGI/ARTI/00/00/06/69/42/LEGIARTI000006694295.xml", "NATURE": "Article", "ORIGINE": "LEGI", "ANCIEN_ID": "SPAOXXXXXXX1X670L03AXXAA" } }, "LIENS": { "LIEN": [ { "@id": "JORFTEXT000000503843", "#text": "Décret 53-1001 1953-10-05 (décret de codification)", "@sens": "source", "@cidtexte": "JORFTEXT000000503843", "@numtexte": "53-1001", "@typelien": "CODIFICATION", "@naturetexte": "DECRET", "@datesignatexte": "1953-10-05" }, { "@id": "LEGIARTI000006696620", "@num": "6", "#text": "Loi n°93-5 du 4 janvier 1993 - art. 6 () JORF 5 janvier 1993", "@sens": "source", "@cidtexte": "JORFTEXT000000178299", "@nortexte": "SPSX9200032L", "@numtexte": "93-5", "@typelien": "CREATION", "@naturetexte": "LOI", "@datesignatexte": "1993-01-04" }, { "@id": "LEGIARTI000006804491", "@num": "Annexe I aux articles R668-1-1 à R668-21", "#text": "Code de la santé publique - art. 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R5106 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006800471", "@num": "R5106-1", "#text": "Code de la santé publique - art. R5106-1 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006799956", "@num": "R5108", "#text": "Code de la santé publique - art. R5108 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006799980", "@num": "R5112-3", "#text": "Code de la santé publique - art. R5112-3 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006800021", "@num": "R5115-1", "#text": "Code de la santé publique - art. R5115-1 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006800505", "@num": "R5115-17", "#text": "Code de la santé publique - art. R5115-17 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "#text": "Loi 58-356 1958-04-03 (loi de validation)", "@sens": "source", "@typelien": "CODIFICATION" } ] }, "CONTEXTE": { "TEXTE": { "TM": { "TM": { "TM": { "TITRE_TM": [ { "@id": "LEGISCTA000006140746", "@fin": "1994-07-30", "#text": "Chapitre 5 : Des médicaments dérivés du sang et du Laboratoire français du fractionnement et des biotechnologies", "@debut": "1993-01-05" } ] }, "TITRE_TM": [ { "@id": "LEGISCTA000006125384", "@fin": "2000-06-22", "#text": "Livre 6 : Utilisation thérapeutique de produits d'origine humaine", "@debut": "1953-10-07" } ] }, "TITRE_TM": [ { "@id": "LEGISCTA000006103420", "@fin": "2999-01-01", "#text": "Partie législative ancienne", "@debut": "1953-10-07" } ] }, "@cid": "LEGITEXT000006072665", "@nature": "CODE", "TITRE_TXT": [ { "@fin": "2999-01-01", "#text": "Code de la santé publique", "@debut": "1953-10-07", "@id_txt": "LEGITEXT000006072665", "@c_titre_court": "Code de la santé publique" } ], "@date_publi": "2999-01-01", "@date_signature": "2999-01-01" } }, "VERSIONS": { "VERSION": [ { "@etat": "MODIFIE", "LIEN_ART": { "@id": "LEGIARTI000006694295", "@fin": "1994-07-30", "@num": "L670-3", "@etat": "MODIFIE", "@debut": "1993-01-05", "@origine": "LEGI" } }, { "@etat": "ABROGE", "LIEN_ART": { "@id": "LEGIARTI000006694296", "@fin": "2000-06-22", "@num": "L670-3", "@etat": "ABROGE", "@debut": "1994-07-30", "@origine": "LEGI" } } ] }, "BLOC_TEXTUEL": { "CONTENU": "
Les règles de la section 1 du chapitre II du titre II du livre V sont applicables au Laboratoire français du fractionnement et des biotechnologies sous réserve des dispositions du présent chapitre et, s'ils vendent en gros des médicaments dérivés du sang, aux établissements de transfusion sanguine, sous réserve des dispositions du chapitre III du présent livre. Le Laboratoire français du fractionnement et des biotechnologies et les établissements concernés doivent être dotés d'un pharmacien responsable qui participe à la direction générale de l'établissement.
\n
" } }, "LEGIARTI000006694296": { "META": { "META_SPEC": { "META_ARTICLE": { "NUM": "L670-3", "ETAT": "ABROGE", "TYPE": "AUTONOME", "DATE_FIN": "2000-06-22", "DATE_DEBUT": "1994-07-30" } }, "META_COMMUN": { "ID": "LEGIARTI000006694296", "URL": "article/LEGI/ARTI/00/00/06/69/42/LEGIARTI000006694296.xml", "NATURE": "Article", "ORIGINE": "LEGI", "ANCIEN_ID": "SPAOXXXXXXX1X670L03AXXAB" } }, "LIENS": { "LIEN": [ { "@id": "JORFTEXT000000503843", "#text": "Décret 53-1001 1953-10-05 (décret de codification)", "@sens": "source", "@cidtexte": "JORFTEXT000000503843", "@numtexte": "53-1001", "@typelien": "CODIFICATION", "@naturetexte": "DECRET", "@datesignatexte": "1953-10-05" }, { "@id": "LEGIARTI000006696772", "@num": "1", "#text": "Loi n°94-654 du 29 juillet 1994 - art. 1 () JORF 30 juillet 1994", "@sens": "source", "@cidtexte": "JORFTEXT000000549618", "@nortexte": "SPSX9400032L", "@numtexte": "94-654", "@typelien": "MODIFICATION", "@naturetexte": "LOI", "@datesignatexte": "1994-07-29" }, { "@id": "LEGIARTI000006696774", "@num": "3", "#text": "Loi n°94-654 du 29 juillet 1994 - art. 3 () JORF 30 juillet 1994", "@sens": "source", "@cidtexte": "JORFTEXT000000549618", "@nortexte": "SPSX9400032L", "@numtexte": "94-654", "@typelien": "MODIFICATION", "@naturetexte": "LOI", "@datesignatexte": "1994-07-29" }, { "@id": "JORFTEXT000000217229", "#text": "Ordonnance 2000-548 2000-06-15 art. 4 I JORF 22 juin 2000", "@sens": "source", "@cidtexte": "JORFTEXT000000217229", "@nortexte": "MESX0000036R", "@typelien": "ABROGATION", "@naturetexte": "RAPPORT", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006804491", "@num": "Annexe I aux articles R668-1-1 à R668-21", "#text": "Code de la santé publique - art. 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R5112-3 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006800021", "@num": "R5115-1", "#text": "Code de la santé publique - art. R5115-1 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006800505", "@num": "R5115-17", "#text": "Code de la santé publique - art. R5115-17 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "CITATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "#text": "Loi 58-356 1958-04-03 (loi de validation)", "@sens": "source", "@typelien": "CODIFICATION" } ] }, "CONTEXTE": { "TEXTE": { "TM": { "TM": { "TM": { "TM": { "TITRE_TM": [ { "@id": "LEGISCTA000006155377", "@fin": "2000-06-22", "#text": "Chapitre 5 : Des médicaments dérivés du sang et du Laboratoire français du fractionnement et des biotechnologies", "@debut": "1994-07-30" } ] }, "TITRE_TM": [ { "@id": "LEGISCTA000006140791", "@fin": "2000-06-22", "#text": "Titre 2 : Du sang humain", "@debut": "1994-07-30" } ] }, "TITRE_TM": [ { "@id": "LEGISCTA000006125383", "@fin": "2000-06-22", "#text": "Livre 6 : Don et utilisation des éléments et produits du corps humain", "@debut": "1994-07-30" } ] }, "TITRE_TM": [ { "@id": "LEGISCTA000006103420", "@fin": "2999-01-01", "#text": "Partie législative ancienne", "@debut": "1953-10-07" } ] }, "@cid": "LEGITEXT000006072665", "@nature": "CODE", "TITRE_TXT": [ { "@fin": "2999-01-01", "#text": "Code de la santé publique", "@debut": "1953-10-07", "@id_txt": "LEGITEXT000006072665", "@c_titre_court": "Code de la santé publique" } ], "@date_publi": "2999-01-01", "@date_signature": "2999-01-01" } }, "VERSIONS": { "VERSION": [ { "@etat": "MODIFIE", "LIEN_ART": { "@id": "LEGIARTI000006694295", "@fin": "1994-07-30", "@num": "L670-3", "@etat": "MODIFIE", "@debut": "1993-01-05", "@origine": "LEGI" } }, { "@etat": "ABROGE", "LIEN_ART": { "@id": "LEGIARTI000006694296", "@fin": "2000-06-22", "@num": "L670-3", "@etat": "ABROGE", "@debut": "1994-07-30", "@origine": "LEGI" } } ] }, "BLOC_TEXTUEL": { "CONTENU": "
Les règles de la section 1 du chapitre II du titre II du livre V sont applicables au Laboratoire français du fractionnement et des biotechnologies sous réserve des dispositions du présent chapitre et, s'ils vendent en gros des médicaments dérivés du sang, aux établissements de transfusion sanguine, sous réserve des dispositions du chapitre III du présent livre. Le Laboratoire français du fractionnement et des biotechnologies et les établissements concernés doivent être dotés d'un pharmacien responsable qui participe à la direction générale de l'établissement.
\n
" } }, "LEGIARTI000006696772": { "META": { "META_SPEC": { "META_ARTICLE": { "NUM": "1", "TYPE": "ENTIEREMENT_MODIF", "DATE_FIN": "2999-01-01", "DATE_DEBUT": "2999-01-01" } }, "META_COMMUN": { "ID": "LEGIARTI000006696772", "URL": "article/LEGI/ARTI/00/00/06/69/67/LEGIARTI000006696772.xml", "NATURE": "Article", "ORIGINE": "LEGI", "ANCIEN_ID": "SPEBXXXXXXX001AAXXXXXXAA" } }, "LIENS": { "LIEN": [ { "@id": "LEGIARTI000006694181", "@num": "L666-1", "#text": "Code de la santé publique - art. L666-1 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "MODIFICATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006694203", "@num": "L666-10", "#text": "Code de la santé publique - art. L666-10 (M)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "MODIFICATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006694206", "@num": "L666-11", "#text": "Code de la santé publique - art. 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L670-4 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "MODIFICATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006694300", "@num": "L670-5", "#text": "Code de la santé publique - art. L670-5 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "MODIFICATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" } ] }, "CONTEXTE": { "TEXTE": { "@cid": "JORFTEXT000000549618", "@nor": "SPSX9400032L", "@num": "94-654", "@nature": "LOI", "TITRE_TXT": [ { "@fin": "2999-01-01", "#text": "LOI no 94-654 du 29 juillet 1994 relative au don et à l'utilisation des éléments et produits du corps humain, à l'assistance médicale à la procréation et au diagnostic prénatal (1)", "@debut": "2999-01-01", "@id_txt": "JORFTEXT000000549618", "@c_titre_court": "Loi n°94-654 du 29 juillet 1994" }, { "@fin": "2999-01-01", "#text": "Loi n° 94-654 du 29 juillet 1994 relative au don et à l'utilisation des éléments et produits du corps humain, à l'assistance médicale à la procréation et au diagnostic prénatal", "@debut": "1994-07-30", "@id_txt": "LEGITEXT000005616306", "@c_titre_court": "Loi n° 94-654 du 29 juillet 1994" } ], "@date_publi": "1994-07-30", "@date_signature": "1994-07-29" } }, "VERSIONS": { "VERSION": [ { "LIEN_ART": { "@id": "LEGIARTI000006696772", "@fin": "2999-01-01", "@num": "1", "@debut": "2999-01-01", "@origine": "LEGI" } } ] }, "BLOC_TEXTUEL": { "CONTENU": "a modifié les dispositions suivantes
\n
" } }, "LEGIARTI000006696774": { "META": { "META_SPEC": { "META_ARTICLE": { "NUM": "3", "TYPE": "ENTIEREMENT_MODIF", "DATE_FIN": "2999-01-01", "DATE_DEBUT": "2999-01-01" } }, "META_COMMUN": { "ID": "LEGIARTI000006696774", "URL": "article/LEGI/ARTI/00/00/06/69/67/LEGIARTI000006696774.xml", "NATURE": "Article", "ORIGINE": "LEGI", "ANCIEN_ID": "SPEBXXXXXXX003AAXXXXXXAA" } }, "LIENS": { "LIEN": [ { "@id": "LEGIARTI000006694181", "@num": "L666-1", "#text": "Code de la santé publique - art. L666-1 (Ab)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "MODIFICATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006694203", "@num": "L666-10", "#text": "Code de la santé publique - art. L666-10 (M)", "@sens": "cible", "@cidtexte": "LEGITEXT000006072665", "@typelien": "MODIFICATION", "@naturetexte": "CODE", "@datesignatexte": "2999-01-01" }, { "@id": "LEGIARTI000006694206", "@num": "L666-11", "#text": "Code de la santé publique - art. 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Sont déterminés par décret en Conseil d'Etat :

\n
\n

1° Les conditions dans lesquelles toute entreprise comportant au moins un établissement pharmaceutique doit être la propriété d'un pharmacien ou d'une société à la gérance ou à la direction de laquelle participe un pharmacien ;

\n
\n

2° Les modalités d'exercice de la location-gérance prévue au premier alinéa de l'article L. 5124-2 ;

\n
\n

3° La durée et le contenu de l'expérience pratique appropriée dont doivent justifier les pharmaciens responsables et les pharmaciens délégués, selon les dispositions du dernier alinéa de l'article L. 5124-2 ;

\n
\n

4° Les modalités d'octroi, de suspension ou de retrait de l'autorisation d'ouverture d'un établissement pharmaceutique prévue à l'article L. 5124-3 ;

\n
\n

5° Les conditions dans lesquelles les établissements publics de santé fabriquant industriellement des médicaments au 31 décembre 1991, peuvent demander à bénéficier de l'autorisation prévue à l'article L. 5124-3 ;

\n
\n

6° Les conditions de remplacement prévu à l'article L. 5124-4 des pharmaciens responsables et des pharmaciens délégués en cas d'absence du titulaire ou s'ils font l'objet d'une interdiction d'exercer ;

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\n

7° Les conditions de la gérance d'un établissement pharmaceutique prévue à l'article L. 5124-4 en cas de décès du pharmacien propriétaire ;

\n
\n

8° Les conditions dans lesquelles peut être faite la publicité en faveur des entreprises et établissements pharmaceutiques ;

\n
\n

9° Les modalités d'application des articles L. 3135-1, L. 5124-7 et L. 5124-8 et les adaptations qui pourront être apportées, en ce qui concerne les établissements pharmaceutiques, aux second, troisième, et quatrième alinéas de l'article L. 5124-2 ;

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10° Les conditions dans lesquelles peut être faite la publicité en faveur des établissements pharmaceutiques ;

\n
\n

11° Les règles régissant l'exportation des médicaments prévue à l'article L. 5124-11 ; \n

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12° Les conditions dans lesquelles l'Agence française de sécurité sanitaire des produits de santé autorise l'importation des médicaments prévue à l'article L. 5124-13 ; \n

\n
\n

13° Les sections de l'ordre auxquelles appartient le pharmacien mentionné à l'article L. 5124-15 et les conditions dans lesquelles ce pharmacien doit être assisté ou remplacé ;

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\n

14° Les conditions dans lesquelles les organismes à but non lucratif et les établissements publics autres que les établissements de santé peuvent bénéficier de l'autorisation visée à l'article L. 5124-3.

\n
" } }, "LEGIARTI000025104409": { "META": { "META_SPEC": { "META_ARTICLE": { "NUM": "L5124-18", "ETAT": "MODIFIE", "TYPE": "AUTONOME", "DATE_FIN": "2016-05-01", "DATE_DEBUT": "2012-05-01" } }, "META_COMMUN": { "ID": "LEGIARTI000025104409", "URL": "article/LEGI/ARTI/00/00/25/10/44/LEGIARTI000025104409.xml", "NATURE": "Article", "ORIGINE": "LEGI" } }, "NOTA": { "CONTENU": "

Loi n° 2011-2012 du 29 décembre 2011 article 41 III : Les présentes dispositions entrent en vigueur à une date prévue par le décret pris pour leur application et au plus tard le 1er août 2012. Dès cette entrée en vigueur, l'Agence nationale de sécurité du médicament et des produits de santé exerce l'ensemble des droits et supporte l'ensemble des obligations de l'Agence française de sécurité sanitaire des produits de santé. Jusqu'à l'entrée en vigueur mentionnée au premier alinéa du présent III, les compétences et pouvoirs que la présente loi attribue à l'Agence nationale de sécurité du médicament et des produits de santé sont exercés par l'Agence française de sécurité sanitaire des produits de santé.

Le décret n° 2012-597 du 27 avril 2012 est entré en vigueur le 1er mai 2012.

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Sont déterminés par décret en Conseil d'Etat :

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\n

2° Les modalités d'exercice de la location-gérance prévue au premier alinéa de l'article L. 5124-2 ;

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4° Les modalités d'octroi, de suspension ou de retrait de l'autorisation d'ouverture d'un établissement pharmaceutique prévue à l'article L. 5124-3 ;

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7° Les conditions de la gérance d'un établissement pharmaceutique prévue à l'article L. 5124-4 en cas de décès du pharmacien propriétaire ;

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\n

8° Les conditions dans lesquelles peut être faite la publicité en faveur des entreprises et établissements pharmaceutiques ;

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10° Les conditions dans lesquelles peut être faite la publicité en faveur des établissements pharmaceutiques ;

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\n

11° Les règles régissant l'exportation des médicaments prévue à l'article L. 5124-11 ; \n

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12° Les conditions dans lesquelles l'Agence nationale de sécurité du médicament et des produits de santé autorise l'importation des médicaments prévue à l'article L. 5124-13 ; \n

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13° Les sections de l'ordre auxquelles appartient le pharmacien mentionné à l'article L. 5124-15 et les conditions dans lesquelles ce pharmacien doit être assisté ou remplacé ;

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\n

\n
" } }, "LEGIARTI000032411571": { "META": { "META_SPEC": { "META_ARTICLE": { "NUM": "L5124-18", "ETAT": "MODIFIE", "TYPE": "AUTONOME", "DATE_FIN": "2019-12-28", "DATE_DEBUT": "2016-05-01" } }, "META_COMMUN": { "ID": "LEGIARTI000032411571", "URL": "article/LEGI/ARTI/00/00/32/41/15/LEGIARTI000032411571.xml", "NATURE": "Article", "ORIGINE": "LEGI" } }, "NOTA": { "CONTENU": "

Le décret n° 2012-597 du 27 avril 2012 est entré en vigueur le 1er mai 2012.

" }, "LIENS": { "LIEN": [ { "@id": "JORFTEXT000000178408", "#text": "Loi 92-1279 1992-12-08 art. 26", "@sens": "source", "@cidtexte": "JORFTEXT000000178408", "@nortexte": "SANX9100161L", "@numtexte": "92-1279", "@typelien": "CONCORDANCE", "@naturetexte": "LOI", "@datesignatexte": "1992-12-08" }, { "@id": "LEGIARTI000006696612", "@num": "26", "#text": "Loi n°92-1279 du 8 décembre 1992 - art. 26 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000000178408", "@nortexte": "SANX9100161L", "@numtexte": "92-1279", "@typelien": "CONCORDE", "@naturetexte": "LOI", "@datesignatexte": "1992-12-08" }, { "@id": "JORFTEXT000000217229", "#text": "Rapport relatif à l'ordonnance n° 2000-548 du 15 juin 2000", "@sens": "source", "@cidtexte": "JORFTEXT000000217229", "@nortexte": "MESX0000036P", "@typelien": "CODIFICATION", "@naturetexte": "RAPPORT", "@datesignatexte": "2999-01-01" }, { "@id": "JORFTEXT000000227015", "#text": "Loi n°2002-303 du 4 mars 2002", "@sens": "source", "@cidtexte": "JORFTEXT000000227015", "@nortexte": "MESX0100092L", "@numtexte": "2002-303", "@typelien": "CODIFICATION", "@naturetexte": "LOI", "@datesignatexte": "2002-03-04" }, { "@id": "LEGIARTI000006232083", "@num": "1", "#text": "Décret n°2004-652 du 2 juillet 2004 - art. 1 (Ab)", "@sens": "cible", "@cidtexte": "JORFTEXT000000436351", "@nortexte": "SANG0421847D", "@numtexte": "2004-652", "@typelien": "CITATION", "@naturetexte": "DECRET", "@datesignatexte": "2004-07-02" }, { "@id": "LEGIARTI000032403211", "@num": "3", "#text": "Ordonnance n°2016-462 du 14 avril 2016 - art. 3 (VD)", "@sens": "cible", "@cidtexte": "JORFTEXT000032402159", "@nortexte": "AFSP1605276R", "@numtexte": "2016-462", "@typelien": "MODIFIE", "@naturetexte": "ORDONNANCE", "@datesignatexte": "2016-04-14" }, { "@id": "LEGIARTI000006915045", "@num": "D5124-57", "#text": "Code de la santé publique - art. 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Sont déterminés par décret en Conseil d'Etat :

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2° Les modalités d'exercice de la location-gérance prévue au premier alinéa de l'article L. 5124-2 ;

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4° Les modalités d'octroi, de suspension ou de retrait de l'autorisation d'ouverture d'un établissement pharmaceutique prévue à l'article L. 5124-3 ;

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7° Les conditions de la gérance d'un établissement pharmaceutique prévue à l'article L. 5124-4 en cas de décès du pharmacien propriétaire ;

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8° Les conditions dans lesquelles peut être faite la publicité en faveur des entreprises et établissements pharmaceutiques ;

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9° Les modalités d'application des articles L. 1413-4, L. 5124-7 et L. 5124-8 et les adaptations qui pourront être apportées, en ce qui concerne les établissements pharmaceutiques, aux second, troisième, et quatrième alinéas de l'article L. 5124-2 ;

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10° Les conditions dans lesquelles peut être faite la publicité en faveur des établissements pharmaceutiques ;

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11° Les règles régissant l'exportation des médicaments prévue à l'article L. 5124-11 ; \n

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12° Les conditions dans lesquelles l'Agence nationale de sécurité du médicament et des produits de santé autorise l'importation des médicaments prévue à l'article L. 5124-13 ; \n

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13° Les sections de l'ordre auxquelles appartient le pharmacien mentionné à l'article L. 5124-15 et les conditions dans lesquelles ce pharmacien doit être assisté ou remplacé ;

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Article L670-5 AUTONOME ABROGE, en vigueur du 30/07/1994 au 22/06/2000 (Code de la santé publique)