Report from the Commission on the experience acquired as a result of the operation of the procedures for granting marketing authorisations for medicinal products laid down in Regulation (EEC) N° 2309/93, in chapter III of directive 75/319/EEC and chapter IV of directive 81/851/EEC Report on the basis of Article 71 of Regulation (EEC) No 2309/93

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Official report CELEX 52001DC0606 from European Union at European Commission. Dated 23 October 2001. Status: open.

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11 official files

• Report from the Commission on the experience acquired as a result of the operation of the procedures for granting marketing authorisations for medicinal products laid down in Regulation (EEC) N° 2309/93, in chapter III of directive 75/319/EEC and chapter IV of directive 81/851/EEC Report on the basis of Article 71 of Regulation (EEC) No 2309/93

  preparatory · EN · 23 October 2001

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• Έκθεση της Επιτροπής σχετικά με την εμπειρία που έχει αποκτηθεί ως αποτέλεσμα της λειτουργίας των διαδικασιών χορήγησης αδειών κυκλοφορίας φαρμακευτικών προϊόντων, όπως ορίζονται στον κανονισμό (ΕΟΚ) αριθ.2309/93, στο κεφάλαιο ΙΙΙ της οδηγίας 75/319/ΕΟΚ και στο κεφάλαιο IV της οδηγίας 81/851/ΕΕC - Έκθεση βάσει του άρθρου 71 του κανονισμού (ΕΟΚ) αριθ. 2309/93

  preparatory · EL · 23 October 2001

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• Bericht der Kommission über die Erfahrungen mit den Verfahren zur Erteilung von Genehmigungen für das Inverkehrbringen von Arzneimitteln gemäß Verordnung (EWG) Nr. 2309/93, Kapitel III der Richtlinie 75/319/EWG und Kapitel IV der Richtlinie 81/851/EWG Bericht gemäß Artikel 71 der Verordnung (EWG) Nr. 2309/93

  preparatory · DE · 23 October 2001

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• Relazione della Commissione Sull'esperienza acquisita nell'applicazione delle procedure per il rilascio delle autorizzazioni all'immissione in commercio dei medicinali stabilite nel Regolamento (CEE) n. 2309/93, nel capitolo III della direttiva 75/319/CEE e nel capitolo IV della direttiva 81/851/CEE Relazione ai sensi dell'articolo 71 del Regolamento (CEE) n. 2309/93

  preparatory · IT · 23 October 2001

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• Beretning fra kommissionen om erfaringerne med de procedurer for tildeling af markedsføringstilladelser til lægemidler, der er fastlagt i forordning (EØF) nr. 2309/93, i kapitel III i direktiv 75/319/EØF og kapitel IV i direktiv 81/851/EØF Rapport udarbejdet på grundlag af artikel 71 i forordning (EØF) nr. 2309/93

  preparatory · DA · 23 October 2001

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• Relatório da Comissão sobre a experiência adquirida em resultado da aplicação dos procedimentos relativos à concessão de autorizações de introdução no mercado de medicamentos estabelecidos no Regulamento (CEE) n.º 2309/93, no capítulo III da Directiva 75/319/CEE e no capítulo IV da Directiva 81/851/CEE Relatório com base no artigo 71.º do Regulamento (CEE) n.º 2309/93

  preparatory · PT · 23 October 2001

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• Rapport de la Commission sur l'expérience acquise dans l'application des procédures d'octroi d'autorisation de mise sur le marché de médicaments fixées dans le règlement (CEE) n° 2309/93, au chapitre III de la directive 75/319/CEE et au chapitre IV de la directive 81/851/CEE Rapport établi en fonction de l'article 71 du règlement (CEE) n° 2309/93

  preparatory · FR · 23 October 2001

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• Verslag van de Commissie over de ervaring die is opgedaan met de toepassing van de procedures voor het verlenen van vergunningen voor het in de handel brengen van geneesmiddelen die zijn vastgesteld in Verordening (EEG) nr. 2309/93, in hoofdstuk III van richtlijn 75/319/EEG en in hoofdstuk IV van richtlijn 81/851/EEG Verslag uit hoofde van artikel 71 van Verordening (EEG) nr. 2309/93

  preparatory · NL · 23 October 2001

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• Informe de la Comisión sobre la experiencia adquirida como resultado de la aplicación de los procedimientos comunitarios para otorgar las autorizaciones de comercialización de medicamentos establecidos en el Reglamento (CEE) nº 2309/93 del Consejo, en el capítulo III de la Directiva 75/319/CEE y en el capítulo IV de la Directiva 81/851/CEE Informe basado en el artículo 71 del Reglamento (CEE) Nº 2309/93

  preparatory · ES · 23 October 2001

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• Kommissionens rapport om de erfarenheter som vunnits vid tillämpningen av de förfaranden för att meddela godkännande för försäljning av läkemedel som fastställs i förordning (EEG) nr 2309/93, kapitel III i direktiv 75/319/EEG och kapitel IV i direktiv 81/851/EEG Rapport grundad på artikel 71 i förordning (EEG) nr 2309/93

  preparatory · SV · 23 October 2001

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• Komission kertomus asetuksessa (ETY) N:o 2309/93, direktiivin 75/319/ETY III luvussa ja direktiivin 81/851/ETY IV luvussa säädettyjen lääkkeiden markkinoille saattamista koskevien lupien myöntämistä koskevista menettelyistä saaduista kokemuksista Asetuksen (ETY) N:o 2309/93 71 artiklan perusteella laadittu kertomus

  preparatory · FI · 23 October 2001

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