Council Directive 87/19/EEC of 22 December 1986 amending Directive 75/318/EEC on the approximation of the laws of the Member States relating to analytical, pharmaco- toxicological and clinical standards and protocols in respect of the testing of proprietary medicinal products

Records

Official directive CELEX 31987L0019 from European Union at EUR-Lex. Dated 22 December 1986. Status: No longer in force.

Timeline

1. 22 December 1986

   Signed

   Source: work_date_document

2. 23 December 1986

   Entry into force

   Source: resource_legal_date_entry-into-force

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Documents

12 official files

• Council Directive 87/19/EEC of 22 December 1986 amending Directive 75/318/EEC on the approximation of the laws of the Member States relating to analytical, pharmaco- toxicological and clinical standards and protocols in respect of the testing of proprietary medicinal products

  official_journal · EN · 22 December 1986

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• Directive 87/19/CEE du Conseil du 22 décembre 1986 modifiant la directive 75/318/CEE relative au rapprochement des législations des États membres concernant les normes et protocoles analytiques, toxico- pharmacologiques et cliniques en matière d'essais de spécialités pharmaceutiques

  official_journal · FR · 22 December 1986

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• Rådets direktiv 87/19/EEG av den 22 december 1986 om ändring av direktivet 75/318/EEG om tillnärmning av medlemsstaternas lagstiftning om analytiska, farmakologiska, toxikologiska och kliniska normer och prövningsplaner vid undersökning av farmaceutiska specialiteter

  official_journal · SV · 22 December 1986

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• Rådets direktiv 87/19/EØF af 22. december 1986 om ændring af direktiv 75/318/EØF om tilnærmelse af medlemsstaternes lovgivning om normer og forskrifter vedrørende analytiske, toksikologisk-farmakologiske og kliniske undersøgelser af farmaceutiske specialiteter

  official_journal · DA · 22 December 1986

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• Richtlinie 87/19/EWG des Rates vom 22. Dezember 1986 zur Änderung der Richtlinie 75/318/EWG zur Angleichung der Rechts- und Verwaltungsvorschriften der Mitgliedstaaten über die analytischen, toxikologisch- pharmakologischen und ärztlichen oder klinischen Vorschriften und Nachweise über Versuche mit Arzneispezialitäten

  official_journal · DE · 22 December 1986

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• Neuvoston direktiivi 87/19/ETY, annettu 22 päivänä joulukuuta 1986, lääkevalmisteiden tutkimiseen liittyviä analyyttisiä, farmakologis-toksikologisia ja kliinisiä standardeja ja tutkimussuunnitelmia koskevan jäsenvaltioiden lainsäädännön lähentämisestä annetun direktiivin 75/318/ETY muuttamisesta

  official_journal · FI · 22 December 1986

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• Directiva 87/19/CEE del Consejo de 22 de diciembre de 1986 por la que se modifica la Directiva 75/318/CEE relativa a la aproximación de las legislaciones de los Estados Miembros sobre normas y protocolos analíticos, tóxico-farmacológicos y clínicos en materia de pruebas de especialidades farmacéuticas

  official_journal · ES · 22 December 1986

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• Οδηγία 87/19/ΕΟΚ του Συμβουλίου της 22ας Δεκεμβρίου 1986 για την τροποποίηση της οδηγίας 75/318/ΕΟΚ περί προσέγγισης των νομοθεσιών των κρατών μελών που αφορούν τις αναλυτικές, τοξικοφαρμακολογικές και κλινικές προδιαγραφές και πρωτόκολλα στον τομέα των δοκιμών των φαρμακευτικών ιδιοσκευασμάτων

  official_journal · EL · 22 December 1986

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• Direttiva 87/19/CEE del Consiglio del 22 dicembre 1986 che modifica la direttiva 75/318/CEE relativa al ravvicinamento delle legislazioni degli Stati Membri riguardanti le norme e i protocolli analitici, tossico- farmacologici e clinici in materia di prove delle specialità medicinali

  official_journal · IT · 22 December 1986

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• Directiva 87/19/CEE do Conselho de 22 de Dezembro de 1986 que altera a Directiva 75/318/CEE relativa à aproximação das legislações dos Estados-Membros respeitantes às normas e protocolos analíticos, tóxico- farmacológicos e clínicos em matéria de ensaios de especialidades farmacêuticas

  official_journal · PT · 22 December 1986

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• Richtlijn 87/19/EEG van de Raad van 22 december 1986 tot wijziging van Richtlijn 75/318/EEG betreffende de onderlinge aanpassing van de wetgevingen van de Lid- Staten inzake de analytische, toxicologisch- farmacologische en klinische normen en voorschriften betreffende proeven op farmaceutische specialiteiten

  official_journal · NL · 22 December 1986

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Sponsors

• · CONSIL · Council of the European Union

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