Information on medicinal products (Community procedures for the authorisation and supervision of medicinal products)

votedEuropean Union· European Parliament· EN

Introduced

24 November 2010

Last action

24 November 2010 · Introduced

Status

PLENARY_VOTE

Official titles

Authentic titles published by the source. The stored canonical title is not replaced.

22 official languages

Bulgarian
Информация относно лекарствени продукти (Процедури на Общността за издаване на разрешения и за контрол върху лекарствените продукти)
Czech
Informace o léčivých přípravcích (postupy Společenství pro registraci léčivých přípravků a dozor nad nimi)
Danish
Oplysninger om lægemidler (fællesskabsprocedurer for godkendelse og overvågning af lægemidler)
German
Informationen über Arzneimittel (Gemeinschaftsverfahren zur Genehmigung und Überwachung von Arzneimitteln)
Greek
Πληροφορίες σχετικά με τα φάρμακα (κοινοτικές διαδικασίες έγκρισης και εποπτείας των φαρμάκων)
Spanish
Informaciones sobre los medicamentos (Procedimientos comunitarios de autorización y supervisión de medicamentos)
Estonian
Teave ravimite kohta (ühenduse kord ravimite lubade andmise ja järelevalve kohta )
Finnish
Lääkkeitä koskeva tiedottaminen (lääkkeitä koskevat yhteisön lupa- ja valvontamenettelyt)
French
Informations sur les médicaments (procédures communautaires pour l'autorisation et la surveillance des médicaments)
Croatian
Informacije o medicinskim proizvodima (postupci Zajednice za odobrenje i nadzor medicinskih proizvoda)
Hungarian
A gyógyszerekre vonatkozó tájékoztatás (közösségi eljárások a gyógyszerek engedélyezése és felügyelete céljából))
Italian
Informazioni relative ai medicinali (Procedure comunitarie per l'autorizzazione e la sorveglianza dei medicinali)
Lithuanian
Informacija apie vaistus (Bendrijos vaistų išdavimo ir priežiūros tvarka)
Latvian
Informācija par zālēm (Kopienas procedūras zāļu reģistrēšanai un uzraudzībai)
Maltese
Informazzjoni dwar prodotti mediċinali (Proċeduri Komunitarji għall-awtorizzazzjoni u s-sorveljanza ta' prodotti mediċinali)
Dutch
Informatie over geneesmiddelen (communautaire procedures voor het verlenen van vergunningen voor en het toezicht op geneesmiddelen)
Polish
Informacje dotyczące produktów leczniczych (wspólnotowe procedury wydawania pozwoleń dla produktów leczniczych i nadzoru nad nimi)
Portuguese
Informações relativas aos medicamentos (Procedimentos comunitários de autorização e fiscalização de medicamentos)
Romanian
Informaţii privind medicamentele (proceduri comunitare pentru autorizarea şi supravegherea medicamentelor)
Slovak
Informácie o liekoch viazaných na lekársky predpis (postupy Spoločenstva pri povoľovaní liekov a pri vykonávaní dozoru nad týmito liekmi)
Slovenian
Informacije o zdravilih (postopki skupnosti za odobritev in nadzor zdravil)
Swedish
Information om läkemedel (gemenskapsförfaranden för godkännande av och tillsyn över läkemedel)

Records

Official bill 2008/0255(COD) from European Union at European Parliament. Dated 24 November 2010. Status: PLENARY_VOTE.

Timeline

24 November 2010
Vote results
Source: PLENARY_VOTE_RESULTS
24 November 2010
Introduced
Information on medicinal products (Community procedures for the authorisation and supervision of medicinal products)
Source: COD

Votes

No vote records are attached yet.

Versions

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Documents

90 official files

RAPORT referitor la propunerea de regulament al Parlamentului European și al Consiliului de modificare a Regulamentului (CE) nr. 726/2004 de stabilire a procedurilor comunitare privind autorizarea și supravegherea medicamentelor de uz uman și veterinar și de instituire a unei Agenții Europene pentru Medicamente, în ceea ce privește informarea publicului larg în privința medicamentelor de uz uman care se eliberează pe bază de prescripții medicale

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RAPORT referitor la propunerea de regulament al Parlamentului European și al Consiliului de modificare a Regulamentului (CE) nr. 726/2004 de stabilire a procedurilor comunitare privind autorizarea și supravegherea medicamentelor de uz uman și veterinar și de instituire a unei Agenții Europene pentru Medicamente, în ceea ce privește informarea publicului larg în privința medicamentelor de uz uman care se eliberează pe bază de prescripții medicale
REPORT_PLENARY · RO · 6 February 2018
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RAPORT referitor la propunerea de regulament al Parlamentului European și al Consiliului de modificare a Regulamentului (CE) nr. 726/2004 de stabilire a procedurilor comunitare privind autorizarea și supravegherea medicamentelor de uz uman și veterinar și de instituire a unei Agenții Europene pentru Medicamente, în ceea ce privește informarea publicului larg în privința medicamentelor de uz uman care se eliberează pe bază de prescripții medicale
REPORT_PLENARY · RO · 6 February 2018
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BERICHT über den Vorschlag für eine Verordnung des Europäischen Parlaments und des Rates zur Änderung der Verordnung (EG) Nr. 726/2004 zur Festlegung von Gemeinschaftsverfahren für die Genehmigung und Überwachung von Human- und Tierarzneimitteln und zur Errichtung einer Europäischen Arzneimittel-Agentur in Bezug auf die Information der breiten Öffentlichkeit über verschreibungspflichtige Humanarzneimittel
REPORT_PLENARY · DE · 6 February 2018
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BERICHT über den Vorschlag für eine Verordnung des Europäischen Parlaments und des Rates zur Änderung der Verordnung (EG) Nr. 726/2004 zur Festlegung von Gemeinschaftsverfahren für die Genehmigung und Überwachung von Human- und Tierarzneimitteln und zur Errichtung einer Europäischen Arzneimittel-Agentur in Bezug auf die Information der breiten Öffentlichkeit über verschreibungspflichtige Humanarzneimittel
REPORT_PLENARY · DE · 6 February 2018
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BERICHT über den Vorschlag für eine Verordnung des Europäischen Parlaments und des Rates zur Änderung der Verordnung (EG) Nr. 726/2004 zur Festlegung von Gemeinschaftsverfahren für die Genehmigung und Überwachung von Human- und Tierarzneimitteln und zur Errichtung einer Europäischen Arzneimittel-Agentur in Bezug auf die Information der breiten Öffentlichkeit über verschreibungspflichtige Humanarzneimittel
REPORT_PLENARY · DE · 6 February 2018
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BERICHT über den Vorschlag für eine Verordnung des Europäischen Parlaments und des Rates zur Änderung der Verordnung (EG) Nr. 726/2004 zur Festlegung von Gemeinschaftsverfahren für die Genehmigung und Überwachung von Human- und Tierarzneimitteln und zur Errichtung einer Europäischen Arzneimittel-Agentur in Bezug auf die Information der breiten Öffentlichkeit über verschreibungspflichtige Humanarzneimittel
REPORT_PLENARY · DE · 6 February 2018
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BETÄNKANDE om förslaget till Europaparlamentets och rådets förordning om ändring i fråga om information till allmänheten om receptbelagda humanläkemedel av förordning (EG) nr 726/2004 om inrättande av gemenskapsförfaranden för godkännande av och tillsyn över humanläkemedel och veterinärmedicinska läkemedel samt om inrättande av en europeisk läkemedelsmyndighet
REPORT_PLENARY · SV · 6 February 2018
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BETÄNKANDE om förslaget till Europaparlamentets och rådets förordning om ändring i fråga om information till allmänheten om receptbelagda humanläkemedel av förordning (EG) nr 726/2004 om inrättande av gemenskapsförfaranden för godkännande av och tillsyn över humanläkemedel och veterinärmedicinska läkemedel samt om inrättande av en europeisk läkemedelsmyndighet
REPORT_PLENARY · SV · 6 February 2018
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BETÄNKANDE om förslaget till Europaparlamentets och rådets förordning om ändring i fråga om information till allmänheten om receptbelagda humanläkemedel av förordning (EG) nr 726/2004 om inrättande av gemenskapsförfaranden för godkännande av och tillsyn över humanläkemedel och veterinärmedicinska läkemedel samt om inrättande av en europeisk läkemedelsmyndighet
REPORT_PLENARY · SV · 6 February 2018
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BETÄNKANDE om förslaget till Europaparlamentets och rådets förordning om ändring i fråga om information till allmänheten om receptbelagda humanläkemedel av förordning (EG) nr 726/2004 om inrättande av gemenskapsförfaranden för godkännande av och tillsyn över humanläkemedel och veterinärmedicinska läkemedel samt om inrättande av en europeisk läkemedelsmyndighet
REPORT_PLENARY · SV · 6 February 2018
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RAPORT Ettepanek võtta vastu Euroopa Parlamendi ja nõukogu määrus, millega muudetakse määrust (EÜ) nr 726/2004 (milles sätestatakse ühenduse kord inim- ja veterinaarravimite lubade andmise ja järelevalve kohta ning millega asutatakse Euroopa Ravimiamet) seoses retsepti alusel väljastatavate inimtervishoius kasutatavate ravimite kohta üldsusele antava teabega
REPORT_PLENARY · ET · 6 February 2018
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RAPORT Ettepanek võtta vastu Euroopa Parlamendi ja nõukogu määrus, millega muudetakse määrust (EÜ) nr 726/2004 (milles sätestatakse ühenduse kord inim- ja veterinaarravimite lubade andmise ja järelevalve kohta ning millega asutatakse Euroopa Ravimiamet) seoses retsepti alusel väljastatavate inimtervishoius kasutatavate ravimite kohta üldsusele antava teabega
REPORT_PLENARY · ET · 6 February 2018
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RAPORT Ettepanek võtta vastu Euroopa Parlamendi ja nõukogu määrus, millega muudetakse määrust (EÜ) nr 726/2004 (milles sätestatakse ühenduse kord inim- ja veterinaarravimite lubade andmise ja järelevalve kohta ning millega asutatakse Euroopa Ravimiamet) seoses retsepti alusel väljastatavate inimtervishoius kasutatavate ravimite kohta üldsusele antava teabega
REPORT_PLENARY · ET · 6 February 2018
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RAPORT Ettepanek võtta vastu Euroopa Parlamendi ja nõukogu määrus, millega muudetakse määrust (EÜ) nr 726/2004 (milles sätestatakse ühenduse kord inim- ja veterinaarravimite lubade andmise ja järelevalve kohta ning millega asutatakse Euroopa Ravimiamet) seoses retsepti alusel väljastatavate inimtervishoius kasutatavate ravimite kohta üldsusele antava teabega
REPORT_PLENARY · ET · 6 February 2018
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RELATÓRIO sobre a proposta de regulamento do Parlamento Europeu e do Conselho que altera, no que diz respeito à informação ao público em geral sobre medicamentos para uso humano sujeitos a receita médica, o Regulamento (CE) n.º 726/2004 que estabelece procedimentos comunitários de autorização e de fiscalização de medicamentos para uso humano e veterinário e que institui uma Agência Europeia de Medicamentos
REPORT_PLENARY · PT · 6 February 2018
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RELATÓRIO sobre a proposta de regulamento do Parlamento Europeu e do Conselho que altera, no que diz respeito à informação ao público em geral sobre medicamentos para uso humano sujeitos a receita médica, o Regulamento (CE) n.º 726/2004 que estabelece procedimentos comunitários de autorização e de fiscalização de medicamentos para uso humano e veterinário e que institui uma Agência Europeia de Medicamentos
REPORT_PLENARY · PT · 6 February 2018
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RELATÓRIO sobre a proposta de regulamento do Parlamento Europeu e do Conselho que altera, no que diz respeito à informação ao público em geral sobre medicamentos para uso humano sujeitos a receita médica, o Regulamento (CE) n.º 726/2004 que estabelece procedimentos comunitários de autorização e de fiscalização de medicamentos para uso humano e veterinário e que institui uma Agência Europeia de Medicamentos
REPORT_PLENARY · PT · 6 February 2018
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RELATÓRIO sobre a proposta de regulamento do Parlamento Europeu e do Conselho que altera, no que diz respeito à informação ao público em geral sobre medicamentos para uso humano sujeitos a receita médica, o Regulamento (CE) n.º 726/2004 que estabelece procedimentos comunitários de autorização e de fiscalização de medicamentos para uso humano e veterinário e que institui uma Agência Europeia de Medicamentos
REPORT_PLENARY · PT · 6 February 2018
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SPRAWOZDANIE w sprawie wniosku dotyczącego rozporządzenia Parlamentu Europejskiego i Rady zmieniającego rozporządzenie (WE) nr 726/2004 ustanawiające wspólnotowe procedury wydawania pozwoleń dla produktów leczniczych stosowanych u ludzi i do celów weterynaryjnych i nadzoru nad nimi oraz ustanawiające Europejską Agencję Leków, w zakresie informacji kierowanych do ogółu społeczeństwa dotyczących produktów leczniczych stosowanych u ludzi i wydawanych na receptę lekarską
REPORT_PLENARY · PL · 6 February 2018
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SPRAWOZDANIE w sprawie wniosku dotyczącego rozporządzenia Parlamentu Europejskiego i Rady zmieniającego rozporządzenie (WE) nr 726/2004 ustanawiające wspólnotowe procedury wydawania pozwoleń dla produktów leczniczych stosowanych u ludzi i do celów weterynaryjnych i nadzoru nad nimi oraz ustanawiające Europejską Agencję Leków, w zakresie informacji kierowanych do ogółu społeczeństwa dotyczących produktów leczniczych stosowanych u ludzi i wydawanych na receptę lekarską
REPORT_PLENARY · PL · 6 February 2018
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SPRAWOZDANIE w sprawie wniosku dotyczącego rozporządzenia Parlamentu Europejskiego i Rady zmieniającego rozporządzenie (WE) nr 726/2004 ustanawiające wspólnotowe procedury wydawania pozwoleń dla produktów leczniczych stosowanych u ludzi i do celów weterynaryjnych i nadzoru nad nimi oraz ustanawiające Europejską Agencję Leków, w zakresie informacji kierowanych do ogółu społeczeństwa dotyczących produktów leczniczych stosowanych u ludzi i wydawanych na receptę lekarską
REPORT_PLENARY · PL · 6 February 2018
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SPRAWOZDANIE w sprawie wniosku dotyczącego rozporządzenia Parlamentu Europejskiego i Rady zmieniającego rozporządzenie (WE) nr 726/2004 ustanawiające wspólnotowe procedury wydawania pozwoleń dla produktów leczniczych stosowanych u ludzi i do celów weterynaryjnych i nadzoru nad nimi oraz ustanawiające Europejską Agencję Leków, w zakresie informacji kierowanych do ogółu społeczeństwa dotyczących produktów leczniczych stosowanych u ludzi i wydawanych na receptę lekarską
REPORT_PLENARY · PL · 6 February 2018
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RAPPORT dwar il-proposta għal regolament tal-Parlament Ewropew u tal-Kunsill li jemenda, fir-rigward tal-informazzjoni għall-pubbliku ġenerali dwar prodotti mediċinali għall-użu tal-bniedem suġġetti għar-riċetta medika, ir-Regolament (KE) Nru 726/2004 li jistabbilixxi proċeduri Komunitarji għall-awtorizzazzjoni u s-sorveljanza ta' prodotti mediċinali għall-użu mill-bniedem u veterinarju u li jistabbilixxi l-Aġenzija Ewropea għall-Mediċini
REPORT_PLENARY · MT · 6 February 2018
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RAPPORT dwar il-proposta għal regolament tal-Parlament Ewropew u tal-Kunsill li jemenda, fir-rigward tal-informazzjoni għall-pubbliku ġenerali dwar prodotti mediċinali għall-użu tal-bniedem suġġetti għar-riċetta medika, ir-Regolament (KE) Nru 726/2004 li jistabbilixxi proċeduri Komunitarji għall-awtorizzazzjoni u s-sorveljanza ta' prodotti mediċinali għall-użu mill-bniedem u veterinarju u li jistabbilixxi l-Aġenzija Ewropea għall-Mediċini
REPORT_PLENARY · MT · 6 February 2018
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RAPPORT dwar il-proposta għal regolament tal-Parlament Ewropew u tal-Kunsill li jemenda, fir-rigward tal-informazzjoni għall-pubbliku ġenerali dwar prodotti mediċinali għall-użu tal-bniedem suġġetti għar-riċetta medika, ir-Regolament (KE) Nru 726/2004 li jistabbilixxi proċeduri Komunitarji għall-awtorizzazzjoni u s-sorveljanza ta' prodotti mediċinali għall-użu mill-bniedem u veterinarju u li jistabbilixxi l-Aġenzija Ewropea għall-Mediċini
REPORT_PLENARY · MT · 6 February 2018
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RAPPORT dwar il-proposta għal regolament tal-Parlament Ewropew u tal-Kunsill li jemenda, fir-rigward tal-informazzjoni għall-pubbliku ġenerali dwar prodotti mediċinali għall-użu tal-bniedem suġġetti għar-riċetta medika, ir-Regolament (KE) Nru 726/2004 li jistabbilixxi proċeduri Komunitarji għall-awtorizzazzjoni u s-sorveljanza ta' prodotti mediċinali għall-użu mill-bniedem u veterinarju u li jistabbilixxi l-Aġenzija Ewropea għall-Mediċini
REPORT_PLENARY · MT · 6 February 2018
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RAPPORT sur la proposition de règlement du Parlement européen et du Conseil modifiant, en ce qui concerne la diffusion auprès du public d'informations relatives aux médicaments à usage humain soumis à prescription médicale, le règlement (CE) n° 726/2004 établissant des procédures communautaires pour l'autorisation et la surveillance en ce qui concerne les médicaments à usage humain et à usage vétérinaire, et instituant une Agence européenne des médicaments
REPORT_PLENARY · FR · 6 February 2018
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RAPPORT sur la proposition de règlement du Parlement européen et du Conseil modifiant, en ce qui concerne la diffusion auprès du public d'informations relatives aux médicaments à usage humain soumis à prescription médicale, le règlement (CE) n° 726/2004 établissant des procédures communautaires pour l'autorisation et la surveillance en ce qui concerne les médicaments à usage humain et à usage vétérinaire, et instituant une Agence européenne des médicaments
REPORT_PLENARY · FR · 6 February 2018
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RAPPORT sur la proposition de règlement du Parlement européen et du Conseil modifiant, en ce qui concerne la diffusion auprès du public d'informations relatives aux médicaments à usage humain soumis à prescription médicale, le règlement (CE) n° 726/2004 établissant des procédures communautaires pour l'autorisation et la surveillance en ce qui concerne les médicaments à usage humain et à usage vétérinaire, et instituant une Agence européenne des médicaments
REPORT_PLENARY · FR · 6 February 2018
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RAPPORT sur la proposition de règlement du Parlement européen et du Conseil modifiant, en ce qui concerne la diffusion auprès du public d'informations relatives aux médicaments à usage humain soumis à prescription médicale, le règlement (CE) n° 726/2004 établissant des procédures communautaires pour l'autorisation et la surveillance en ce qui concerne les médicaments à usage humain et à usage vétérinaire, et instituant une Agence européenne des médicaments
REPORT_PLENARY · FR · 6 February 2018
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ДОКЛАД относно предложението за регламент на Европейския парламент и на Съвета за изменение на Регламент (ЕО) № 726/2004 за установяване на процедури на Общността за разрешаване и контрол на лекарствени продукти за хуманна и ветеринарна употреба и за създаване на Европейска агенция по лекарствата по отношение на предоставянето на информация за широката общественост относно лекарствени продукти за хуманна употреба, отпускани по лекарско предписание
REPORT_PLENARY · BG · 6 February 2018
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ДОКЛАД относно предложението за регламент на Европейския парламент и на Съвета за изменение на Регламент (ЕО) № 726/2004 за установяване на процедури на Общността за разрешаване и контрол на лекарствени продукти за хуманна и ветеринарна употреба и за създаване на Европейска агенция по лекарствата по отношение на предоставянето на информация за широката общественост относно лекарствени продукти за хуманна употреба, отпускани по лекарско предписание
REPORT_PLENARY · BG · 6 February 2018
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ДОКЛАД относно предложението за регламент на Европейския парламент и на Съвета за изменение на Регламент (ЕО) № 726/2004 за установяване на процедури на Общността за разрешаване и контрол на лекарствени продукти за хуманна и ветеринарна употреба и за създаване на Европейска агенция по лекарствата по отношение на предоставянето на информация за широката общественост относно лекарствени продукти за хуманна употреба, отпускани по лекарско предписание
REPORT_PLENARY · BG · 6 February 2018
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ДОКЛАД относно предложението за регламент на Европейския парламент и на Съвета за изменение на Регламент (ЕО) № 726/2004 за установяване на процедури на Общността за разрешаване и контрол на лекарствени продукти за хуманна и ветеринарна употреба и за създаване на Европейска агенция по лекарствата по отношение на предоставянето на информация за широката общественост относно лекарствени продукти за хуманна употреба, отпускани по лекарско предписание
REPORT_PLENARY · BG · 6 February 2018
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BERICHT über den Vorschlag für eine Verordnung des Europäischen Parlaments und des Rates zur Änderung der Verordnung (EG) Nr. 726/2004 zur Festlegung von Gemeinschaftsverfahren für die Genehmigung und Überwachung von Human- und Tierarzneimitteln und zur Errichtung einer Europäischen Arzneimittel-Agentur in Bezug auf die Information der breiten Öffentlichkeit über verschreibungspflichtige Humanarzneimittel
REPORT_PLENARY · EN · 30 January 2018
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BERICHT über den Vorschlag für eine Verordnung des Europäischen Parlaments und des Rates zur Änderung der Verordnung (EG) Nr. 726/2004 zur Festlegung von Gemeinschaftsverfahren für die Genehmigung und Überwachung von Human- und Tierarzneimitteln und zur Errichtung einer Europäischen Arzneimittel-Agentur in Bezug auf die Information der breiten Öffentlichkeit über verschreibungspflichtige Humanarzneimittel
REPORT_PLENARY · EN · 30 January 2018
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BERICHT über den Vorschlag für eine Verordnung des Europäischen Parlaments und des Rates zur Änderung der Verordnung (EG) Nr. 726/2004 zur Festlegung von Gemeinschaftsverfahren für die Genehmigung und Überwachung von Human- und Tierarzneimitteln und zur Errichtung einer Europäischen Arzneimittel-Agentur in Bezug auf die Information der breiten Öffentlichkeit über verschreibungspflichtige Humanarzneimittel
REPORT_PLENARY · EN · 30 January 2018
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BERICHT über den Vorschlag für eine Verordnung des Europäischen Parlaments und des Rates zur Änderung der Verordnung (EG) Nr. 726/2004 zur Festlegung von Gemeinschaftsverfahren für die Genehmigung und Überwachung von Human- und Tierarzneimitteln und zur Errichtung einer Europäischen Arzneimittel-Agentur in Bezug auf die Information der breiten Öffentlichkeit über verschreibungspflichtige Humanarzneimittel
REPORT_PLENARY · EN · 30 January 2018
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Suite donnée au T7-0430/2010
ACT_FOLLOWUP · FR · 21 March 2011
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Follow up to T7-0430/2010
ACT_FOLLOWUP · EN · 10 March 2011
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Official source: https://oeil.secure.europarl.europa.eu/oeil/popups/ficheprocedure.do?lang=en&reference=2008%2F0255(COD)
Open data entity: https://data.europarl.europa.eu/api/v2/procedures/2008-0255
eu · 2008-0255 · source updated 24 November 2010