Supplementary protection certificate for medicinal products (recast)

votedEuropean Union· European Parliament· EN

Introduced

11 September 2023

Last action

28 February 2024 · Plenary vote

Status

PLENARY_VOTE

Official titles

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

23 official languages

Bulgarian
Сертификат за допълнителна закрила на лекарствените продукти (преработен текст)
Czech
Dodatkové ochranné osvědčení pro léčivé přípravky (přepracované znění)
Danish
Supplerende beskyttelsescertifikat for lægemidler (omarbejdning)
German
Ergänzendes Schutzzertifikat für Arzneimittel (Neufassung)
Greek
Συμπληρωματικό πιστοποιητικό προστασίας για τα φάρμακα (αναδιατύπωση)
Spanish
Certificado complementario de protección para los medicamentos (versión refundida)
Estonian
Ravimite täiendava kaitse tunnistus (uuesti sõnastatud)
Finnish
Lääkkeiden lisäsuojatodistus (uudelleenlaadittu)
French
Certificat complémentaire de protection pour les médicaments (refonte)
Irish
Deimhniú forlíontach cosanta le haghaidh táirgí íocshláinte (athmhúnlú)
Croatian
Svjedodžba o dodatnoj zaštiti za lijekove (preinaka)
Hungarian
A gyógyszerek kiegészítő oltalmi tanúsítványa (átdolgozás)
Italian
Certificato protettivo complementare per i medicinali (rifusione)
Lithuanian
Medicinos produktų papildomos apsaugos liudijimas (nauja redakcija)
Latvian
Papildu aizsardzības sertifikāts zālēm (pārstrādāta redakcija)
Maltese
Ċertifikat ta’ protezzjoni supplimentari għal prodotti mediċinali (riformulazzjoni)
Dutch
Aanvullend beschermingscertificaat voor geneesmiddelen (herschikking)
Polish
Dodatkowe świadectwo ochronne dla produktów leczniczych (wersja przekształcona)
Portuguese
Certificado complementar de proteção para produtos medicinais (reformulação)
Romanian
Certificatul suplimentar de protecție pentru medicamente (reformare)
Slovak
Dodatkové ochranné osvedčenie pre lieky (prepracované znenie)
Slovenian
Dodatni varstveni certifikat za zdravila (prenovitev)
Swedish
Tilläggsskydd för läkemedel (omarbetning)

Records

Official bill 2023/0130(COD) from European Union at European Parliament. Dated 11 September 2023. Status: PLENARY_VOTE.

Timeline

11 September 2023
referral
Source: REFERRAL
11 September 2023
Introduced
Supplementary protection certificate for medicinal products (recast)
Source: COD
13 October 2023
committee tabling report
Source: COMMITTEE_TABLING_REPORT
7 November 2023
committee adopting opinion
Source: COMMITTEE_ADOPTING_OPINION
14 November 2023
committee tabling amendment
Source: COMMITTEE_TABLING_AMENDMENT
24 January 2024
committee adopting report
Source: COMMITTEE_ADOPTING_REPORT
1 February 2024
tabling plenary
Source: TABLING_PLENARY
27 February 2024
Plenary debate
Source: PLENARY_DEBATE
27 February 2024
Plenary debate
Source: PLENARY_DEBATE
28 February 2024
Vote results
Source: PLENARY_VOTE_RESULTS
28 February 2024
plenary amend proposal
Source: PLENARY_AMEND_PROPOSAL
28 February 2024
Plenary vote
Source: PLENARY_VOTE
28 February 2024
Plenary vote
Source: PLENARY_VOTE

Votes

No vote records are attached yet.

Versions

No version snapshots stored. Document URLs remain at the source.

Documents

415 official files

IZVJEŠĆE o Prijedlogu uredbe Europskog parlamenta i Vijeća o svjedodžbi o dodatnoj zaštiti za lijekove (preinaka)

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IZVJEŠĆE o Prijedlogu uredbe Europskog parlamenta i Vijeća o svjedodžbi o dodatnoj zaštiti za lijekove (preinaka)
REPORT_PLENARY · HR · 14 February 2024
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ZPRÁVA o návrhu nařízení Evropského parlamentu a Rady o jednotném dodatkovém osvědčení pro léčivé přípravky a o změně nařízení (EU) 2017/1001, nařízení (ES) č. 1901/2006 a nařízení (EU) č. 608/2013
REPORT_PLENARY · CS · 14 February 2024
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ZPRÁVA o návrhu nařízení Evropského parlamentu a Rady o jednotném dodatkovém osvědčení pro léčivé přípravky a o změně nařízení (EU) 2017/1001, nařízení (ES) č. 1901/2006 a nařízení (EU) č. 608/2013
REPORT_PLENARY · CS · 14 February 2024
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RAPPORT dwar il-proposta għal regolament tal-Parlament Ewropew u tal-Kunsill dwar iċ-ċertifikat ta’ protezzjoni supplimentari għal prodotti mediċinali (riformulazzjoni)
REPORT_PLENARY · MT · 14 February 2024
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RAPPORT dwar il-proposta għal regolament tal-Parlament Ewropew u tal-Kunsill dwar iċ-ċertifikat ta’ protezzjoni supplimentari għal prodotti mediċinali (riformulazzjoni)
REPORT_PLENARY · MT · 14 February 2024
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SPRÁVA o návrhu nariadenia Európskeho parlamentu a Rady o jednotnom dodatkovom ochrannom osvedčení pre lieky, ktorým sa mení nariadenie (EÚ) 2017/1001, nariadenie (ES) č. 1901/2006, ako aj nariadenie (EÚ) č. 608/2013
REPORT_PLENARY · SK · 14 February 2024
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SPRÁVA o návrhu nariadenia Európskeho parlamentu a Rady o jednotnom dodatkovom ochrannom osvedčení pre lieky, ktorým sa mení nariadenie (EÚ) 2017/1001, nariadenie (ES) č. 1901/2006, ako aj nariadenie (EÚ) č. 608/2013
REPORT_PLENARY · SK · 14 February 2024
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BETÆNKNING om forslag til Europa-Parlamentets og Rådets forordning om det supplerende beskyttelsescertifikat for lægemidler (omarbejdning)
REPORT_PLENARY · DA · 14 February 2024
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BETÆNKNING om forslag til Europa-Parlamentets og Rådets forordning om det supplerende beskyttelsescertifikat for lægemidler (omarbejdning)
REPORT_PLENARY · DA · 14 February 2024
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RAPORT ettepaneku kohta võtta vastu Euroopa Parlamendi ja nõukogu määrus, mis käsitleb standardi rakendamiseks olulisi patente ja millega muudetakse määrust (EL) 2017/1001
REPORT_PLENARY · ET · 13 February 2024
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RAPORT ettepaneku kohta võtta vastu Euroopa Parlamendi ja nõukogu määrus, mis käsitleb standardi rakendamiseks olulisi patente ja millega muudetakse määrust (EL) 2017/1001
REPORT_PLENARY · ET · 13 February 2024
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RELATÓRIO sobre a proposta de regulamento do Parlamento Europeu e do Conselho relativo ao certificado complementar de proteção unitário para os medicamentos, e que altera o Regulamento (UE) 2017/1001, o Regulamento (CE) n.º 1901/2006, bem como o Regulamento (UE) n.º 608/2013
REPORT_PLENARY · PT · 13 February 2024
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RELATÓRIO sobre a proposta de regulamento do Parlamento Europeu e do Conselho relativo ao certificado complementar de proteção unitário para os medicamentos, e que altera o Regulamento (UE) 2017/1001, o Regulamento (CE) n.º 1901/2006, bem como o Regulamento (UE) n.º 608/2013
REPORT_PLENARY · PT · 13 February 2024
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RAPORT referitor la propunerea de regulament al Parlamentului European și al Consiliului privind brevetele esențiale pentru standarde și de modificare a Regulamentului (UE) 2017/1001
REPORT_PLENARY · RO · 13 February 2024
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RAPORT referitor la propunerea de regulament al Parlamentului European și al Consiliului privind brevetele esențiale pentru standarde și de modificare a Regulamentului (UE) 2017/1001
REPORT_PLENARY · RO · 13 February 2024
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RELATÓRIO sobre a proposta de regulamento do Parlamento Europeu e do Conselho relativo a patentes essenciais a normas que altera o Regulamento (UE) 2017/1001
REPORT_PLENARY · PT · 13 February 2024
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RELATÓRIO sobre a proposta de regulamento do Parlamento Europeu e do Conselho relativo a patentes essenciais a normas que altera o Regulamento (UE) 2017/1001
REPORT_PLENARY · PT · 13 February 2024
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BERICHT über den Vorschlag für eine Verordnung des Europäischen Parlaments und des Rates über standardessenzielle Patente und zur Änderung der Verordnung (EU) 2017/1001
REPORT_PLENARY · DE · 13 February 2024
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BERICHT über den Vorschlag für eine Verordnung des Europäischen Parlaments und des Rates über standardessenzielle Patente und zur Änderung der Verordnung (EU) 2017/1001
REPORT_PLENARY · DE · 13 February 2024
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POROČILO o predlogu uredbe Evropskega parlamenta in Sveta o za standard bistvenih patentih in spremembi Uredbe (EU) 2017/1001
REPORT_PLENARY · SL · 13 February 2024
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POROČILO o predlogu uredbe Evropskega parlamenta in Sveta o za standard bistvenih patentih in spremembi Uredbe (EU) 2017/1001
REPORT_PLENARY · SL · 13 February 2024
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TUARASCÁIL ar an togra le haghaidh Rialachán ó Pharlaimint na hEorpa agus ón gComhairle maidir le bunphaitinní caighdeáin agus lena leasaítear Rialachán (AE)2017/1001
REPORT_PLENARY · GA · 13 February 2024
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TUARASCÁIL ar an togra le haghaidh Rialachán ó Pharlaimint na hEorpa agus ón gComhairle maidir le bunphaitinní caighdeáin agus lena leasaítear Rialachán (AE)2017/1001
REPORT_PLENARY · GA · 13 February 2024
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RELAZIONE sulla proposta di regolamento del Parlamento europeo e del Consiglio relativo ai brevetti essenziali, che modifica il regolamento (UE) 2017/1001
REPORT_PLENARY · IT · 13 February 2024
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RELAZIONE sulla proposta di regolamento del Parlamento europeo e del Consiglio relativo ai brevetti essenziali, che modifica il regolamento (UE) 2017/1001
REPORT_PLENARY · IT · 13 February 2024
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SPRAWOZDANIE w sprawie rozporządzenia Parlamentu Europejskiego i Rady w sprawie patentów niezbędnych do spełnienia normy oraz zmieniającego rozporządzenie (UE) 2017/1001
REPORT_PLENARY · PL · 13 February 2024
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SPRAWOZDANIE w sprawie rozporządzenia Parlamentu Europejskiego i Rady w sprawie patentów niezbędnych do spełnienia normy oraz zmieniającego rozporządzenie (UE) 2017/1001
REPORT_PLENARY · PL · 13 February 2024
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RAPPORT dwar il-proposta għal regolament tal-Parlament Ewropew u tal-Kunsill dwar privattivi essenzjali standard u li jemenda r-Regolament (UE) 2017/1001
REPORT_PLENARY · MT · 13 February 2024
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RAPPORT dwar il-proposta għal regolament tal-Parlament Ewropew u tal-Kunsill dwar privattivi essenzjali standard u li jemenda r-Regolament (UE) 2017/1001
REPORT_PLENARY · MT · 13 February 2024
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RELAZIONE sulla proposta di regolamento del Parlamento europeo e del Consiglio sul certificato protettivo complementare per i medicinali (rifusione)
REPORT_PLENARY · IT · 13 February 2024
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RELAZIONE sulla proposta di regolamento del Parlamento europeo e del Consiglio sul certificato protettivo complementare per i medicinali (rifusione)
REPORT_PLENARY · IT · 13 February 2024
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IZVJEŠĆE o Prijedlogu uredbe Europskog parlamenta i Vijeća o patentima bitnima za normu i izmjeni Uredbe (EU) 2017/1001
REPORT_PLENARY · HR · 13 February 2024
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IZVJEŠĆE o Prijedlogu uredbe Europskog parlamenta i Vijeća o patentima bitnima za normu i izmjeni Uredbe (EU) 2017/1001
REPORT_PLENARY · HR · 13 February 2024
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SPRÁVA o návrhu nariadenia Európskeho parlamentu a Rady o patentoch nevyhnutných pre normy, ktorým sa mení nariadenie (EÚ) 2017/1001
REPORT_PLENARY · SK · 13 February 2024
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SPRÁVA o návrhu nariadenia Európskeho parlamentu a Rady o patentoch nevyhnutných pre normy, ktorým sa mení nariadenie (EÚ) 2017/1001
REPORT_PLENARY · SK · 13 February 2024
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VERSLAG over het voorstel voor een verordening van het Europees Parlement en de Raad betreffende standaardessentiële octrooien en tot wijziging van Verordening (EU) 2017/1001
REPORT_PLENARY · NL · 13 February 2024
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VERSLAG over het voorstel voor een verordening van het Europees Parlement en de Raad betreffende standaardessentiële octrooien en tot wijziging van Verordening (EU) 2017/1001
REPORT_PLENARY · NL · 13 February 2024
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ДОКЛАД относно предложението за регламент на Европейския парламент и на Съвета относно патентите от съществено значение за стандарт и за изменение на Регламент (ЕС) 2017/1001
REPORT_PLENARY · BG · 13 February 2024
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ДОКЛАД относно предложението за регламент на Европейския парламент и на Съвета относно патентите от съществено значение за стандарт и за изменение на Регламент (ЕС) 2017/1001
REPORT_PLENARY · BG · 13 February 2024
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BETÆNKNING om forslag til Europa-Parlamentets og Rådets forordning om det fælles supplerende beskyttelsescertifikat for lægemidler og om ændring af forordning (EU) 2017/1001, forordning (EF) nr. 1901/2006 og forordning (EU) nr. 608/2013
REPORT_PLENARY · DA · 13 February 2024
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BETÆNKNING om forslag til Europa-Parlamentets og Rådets forordning om det fælles supplerende beskyttelsescertifikat for lægemidler og om ændring af forordning (EU) 2017/1001, forordning (EF) nr. 1901/2006 og forordning (EU) nr. 608/2013
REPORT_PLENARY · DA · 13 February 2024
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ZIŅOJUMS par priekšlikumu Eiropas Parlamenta un Padomes regulai par standartam būtiskiem patentiem un ar ko groza Regulu (ES) 2017/1001
REPORT_PLENARY · LV · 13 February 2024
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ZIŅOJUMS par priekšlikumu Eiropas Parlamenta un Padomes regulai par standartam būtiskiem patentiem un ar ko groza Regulu (ES) 2017/1001
REPORT_PLENARY · LV · 13 February 2024
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POROČILO o predlogu uredbe Evropskega parlamenta in Sveta o dodatnem varstvenem certifikatu za zdravila (prenovitev)
REPORT_PLENARY · SL · 13 February 2024
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POROČILO o predlogu uredbe Evropskega parlamenta in Sveta o dodatnem varstvenem certifikatu za zdravila (prenovitev)
REPORT_PLENARY · SL · 13 February 2024
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PRANEŠIMAS dėl pasiūlymo dėl Europos Parlamento ir Tarybos reglamento dėl esminių standartų patentų, kuriuo iš dalies keičiamas Reglamentas (ES) 2017/1001
REPORT_PLENARY · LT · 13 February 2024
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PRANEŠIMAS dėl pasiūlymo dėl Europos Parlamento ir Tarybos reglamento dėl esminių standartų patentų, kuriuo iš dalies keičiamas Reglamentas (ES) 2017/1001
REPORT_PLENARY · LT · 13 February 2024
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ΕΚΘΕΣΗ σχετικά με την πρόταση κανονισμού του Ευρωπαϊκού Κοινοβουλίου και του Συμβουλίου που αφορά τα ουσιώδη για τη λειτουργία προτύπου διπλώματα ευρεσιτεχνίας και την τροποποίηση του κανονισμού (ΕΕ) 2017/1001
REPORT_PLENARY · EL · 13 February 2024
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ΕΚΘΕΣΗ σχετικά με την πρόταση κανονισμού του Ευρωπαϊκού Κοινοβουλίου και του Συμβουλίου που αφορά τα ουσιώδη για τη λειτουργία προτύπου διπλώματα ευρεσιτεχνίας και την τροποποίηση του κανονισμού (ΕΕ) 2017/1001
REPORT_PLENARY · EL · 13 February 2024
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JELENTÉS a szabványmegfelelőségi szempontból elengedhetetlen szabadalmakról és az (EU) 2017/1001 rendelet módosításáról szóló európai parlamenti és tanácsi rendeletre irányuló javaslatról
REPORT_PLENARY · HU · 13 February 2024
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Official source: https://oeil.secure.europarl.europa.eu/oeil/popups/ficheprocedure.do?lang=en&reference=2023%2F0130(COD)
Open data entity: https://data.europarl.europa.eu/api/v2/procedures/2023-0130
eu · 2023-0130 · source updated 28 February 2024