European Union · Directive · L
CELEX 31975L0318
Council Directive 75/318/EEC of 20 May 1975 on the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of proprietary medicinal products
Introduced
20 May 1975
Last action
21 May 1975 · Entry into force
Status
No longer in force
Sponsors
—
Subjects
Discovery layer
Source updated
20 May 1975
Records
Official directive CELEX 31975L0318 from European Union at EUR-Lex. Dated 20 May 1975. Status: No longer in force.
Timeline
20 May 1975
Signed
Source: work_date_document
21 May 1975
Entry into force
Source: resource_legal_date_entry-into-force
Votes
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Versions
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Documents
12 official files
Richtlinie 75/318/EWG des Rates vom 20. Mai 1975 zur Angleichung der Rechts- und Verwaltungsvorschriften der Mitgliedstaaten über die analytischen, toxikologisch- pharmakologischen und ärtzlichen oder klinischen Vorschriften und Nachweise über Versuche mit Arzneimittelspezialitäten
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Richtlinie 75/318/EWG des Rates vom 20. Mai 1975 zur Angleichung der Rechts- und Verwaltungsvorschriften der Mitgliedstaaten über die analytischen, toxikologisch- pharmakologischen und ärtzlichen oder klinischen Vorschriften und Nachweise über Versuche mit Arzneimittelspezialitäten
official_journal · DE · 20 May 1975
Neuvoston direktiivi 75/318/ETY, annettu 20 päivänä toukokuuta 1975, lääkevalmisteiden tutkimiseen liittyviä analyyttisiä, farmakologis-toksikologisia ja kliinisiä standardeja ja tutkimussuunnitelmia koskevan jäsenvaltioiden lainsäädännön lähentämisestä
official_journal · FI · 20 May 1975
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Direttiva 75/318/CEE del Consiglio, del 20 maggio 1975, relativa al ravvicinamento delle legislazioni degli Stati Membri riguardanti le norme ed i protocolli analitici, tossicofarmacologici e clinici in materia di sperimentazione delle specialità medicinali
official_journal · IT · 20 May 1975
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Directiva 75/318/CEE del Consejo, de 20 de mayo de 1975, 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 · 20 May 1975
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Rådets direktiv 75/318/EØF af 20. maj 1975 om tilnærmelse af medlemsstaternes lovgivning om normer og forskrifter vedrørende analytiske, toksikologisk- farmakologiske og kliniske undersøgelser af medicinske specialiteter
official_journal · DA · 20 May 1975
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Directive 75/318/CEE du Conseil, du 20 mai 1975, 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 · 20 May 1975
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Directiva 75/318/CEE do Conselho, de 20 de Maio de 1975, 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 · 20 May 1975
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Οδηγία 75/318/ΕΟΚ του Συμβουλίου της 20ής Μαΐου 1975 περί της προσεγγίσεως 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 · 20 May 1975
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Rådets direktiv 75/318/EEG av den 20 maj 1975 om tillnärmning av medlemsstaternas lagstiftning om analytiska, farmakologiska, toxikologiska och kliniska normer och prövningsplaner för undersökning av farmaceutiska specialiteter
official_journal · SV · 20 May 1975
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Richtlijn 75/318/EEG van de Raad van 20 mei 1975 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 · 20 May 1975
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Council Directive 75/318/EEC of 20 May 1975 on the approximation of the laws of Member States relating to analytical, pharmaco-toxicological and clinical standards and protocols in respect of the testing of proprietary medicinal products
official_journal · EN · 20 May 1975
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Sponsors
- · CONSIL · Council of the European Union
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Sources
PoliticalRepo is an index and interpretation layer, not the authoritative legal source.
- Official source: https://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX:31975L0318
- Open data entity: http://publications.europa.eu/resource/cellar/845d1ac1-0b12-4d7f-8cbc-821ae51a6b2d
- eurlex · 31975L0318 · source updated 20 May 1975