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Working Party on Pharmaceuticals and Medical Devices Date: 8 and 9 April 2024 Time: 10:00, 10:00 Venue: COUNCIL LEX BUILDING Rue de la Loi 145, 1048 BRUSSELS (178671/EU XXVII.GP)

EU-V: Tagesordnung

Working Party on Pharmaceuticals and Medical Devices Date: 8 and 9 April 2024 Time: 10:00, 10:00 Venue: COUNCIL LEX BUILDING Rue de la Loi 145, 1048 BRUSSELS

Gruppe: Gruppe "Arzneimittel und Medizinprodukte"

betrifft Sitzungen am 08.04.2024 und 09.04.2024

Erstellt am 26.03.2024 von: Gesundheit

Eingelangt am 26.03.2024, U32 Übermittlung

RAT: CM 2258/24
PDF

Linkart	Link
RAT Rat	8216/24
RAT Rat	8232/24
RAG Ratsarbeitsgruppen	Gruppe "Arzneimittel und Medizinprodukte"
RIL Richtlinien	2001/83/EC
RIL Richtlinien	2009/35/EC
VER Verordnungen	1394/2007
VER Verordnungen	141/2000
VER Verordnungen	1901/2006
VER Verordnungen	536/2014
VER Verordnungen	726/2004

Datum	Dok.Nr. Dokumenten der EU-Institutionen zugeordnete, fortlaufende Nummer mit Jahreszahl, um diese eindeutig zu identifizieren.	Art	Betreff
02.04.2024	RAT: 8216/24	EUST EU-Vorlage: Offizielles Ratsdokument	Proposal for a Regulation of the European Parliament and of the Council laying down Union procedures for the authorisation and supervision of medicinal products for human use and establishing rules governing the European Medicines Agency, amending Regulation (EC) No 1394/2007 and Regulation (EU) No 536/2014 and repealing Regulation (EC) No 726/2004, Regulation (EC) No 141/2000 and Regulation (EC) No 1901/2006 Proposal for a Directive of the European Parliament and of the Council on the Union code relating to medicinal products for human use, and repealing Directive 2001/83/EC and Directive 2009/35/EC - Exchange of views (179053/EU XXVII.GP)
02.04.2024	RAT: 8232/24	EUST EU-Vorlage: Offizielles Ratsdokument	Proposal for a Regulation of the European Parliament and of the Council laying down Union procedures for the authorisation and supervision of medicinal products for human use and establishing rules governing the European Medicines Agency, amending Regulation (EC) No 1394/2007 and Regulation (EU) No 536/2014 and repealing Regulation (EC) No 726/2004, Regulation (EC) No 141/2000 and Regulation (EC) No 1901/2006 Proposal for a Directive of the European Parliament and of the Council on the Union code relating to medicinal products for human use, and repealing Directive 2001/83/EC and Directive 2009/35/EC - Exchange of views (179057/EU XXVII.GP)
02.04.2024	RAT: 8232/24	EUST EU-Vorlage: Offizielles Ratsdokument	Proposal for a Regulation of the European Parliament and of the Council laying down Union procedures for the authorisation and supervision of medicinal products for human use and establishing rules governing the European Medicines Agency, amending Regulation (EC) No 1394/2007 and Regulation (EU) No 536/2014 and repealing Regulation (EC) No 726/2004, Regulation (EC) No 141/2000 and Regulation (EC) No 1901/2006 Proposal for a Directive of the European Parliament and of the Council on the Union code relating to medicinal products for human use, and repealing Directive 2001/83/EC and Directive 2009/35/EC - Exchange of views (179057/EU XXVII.GP)
02.04.2024	RAT: 8216/24	EUST EU-Vorlage: Offizielles Ratsdokument	Proposal for a Regulation of the European Parliament and of the Council laying down Union procedures for the authorisation and supervision of medicinal products for human use and establishing rules governing the European Medicines Agency, amending Regulation (EC) No 1394/2007 and Regulation (EU) No 536/2014 and repealing Regulation (EC) No 726/2004, Regulation (EC) No 141/2000 and Regulation (EC) No 1901/2006 Proposal for a Directive of the European Parliament and of the Council on the Union code relating to medicinal products for human use, and repealing Directive 2001/83/EC and Directive 2009/35/EC - Exchange of views (179053/EU XXVII.GP)
08.04.2024	RAT: WK 5056/24	EUB EU-Vorlage Berichte u. Beratungsergebnisse	Unmet medical need (UMN) and high unmet medical need (HUMN) criteria in the proposed pharmaceutical reform/Presentation by the Commission (181056/EU XXVII.GP)
08.04.2024	RAT: WK 5056/24	EUB EU-Vorlage Berichte u. Beratungsergebnisse	Unmet medical need (UMN) and high unmet medical need (HUMN) criteria in the proposed pharmaceutical reform/Presentation by the Commission (181056/EU XXVII.GP)
09.04.2024	RAT: WK 5008/24	EUB EU-Vorlage Berichte u. Beratungsergebnisse	Pharma package – clusters shortages and incentives/Presentations by the Presidency (181055/EU XXVII.GP)
09.04.2024	RAT: WK 5008/24	EUB EU-Vorlage Berichte u. Beratungsergebnisse	Pharma package – clusters shortages and incentives/Presentations by the Presidency (181055/EU XXVII.GP)

Dok.Nr.

Betreff

RAT: 8216/24

Proposal for a Regulation of the European Parliament and of the Council laying down Union procedures for the authorisation and supervision of medicinal products for human use and establishing rules governing the European Medicines Agency, amending Regulation (EC) No 1394/2007 and Regulation (EU) No 536/2014 and repealing Regulation (EC) No 726/2004, Regulation (EC) No 141/2000 and Regulation (EC) No 1901/2006 Proposal for a Directive of the European Parliament and of the Council on the Union code relating to medicinal products for human use, and repealing Directive 2001/83/EC and Directive 2009/35/EC - Exchange of views (179053/EU XXVII.GP)

RAT: 8232/24

Proposal for a Regulation of the European Parliament and of the Council laying down Union procedures for the authorisation and supervision of medicinal products for human use and establishing rules governing the European Medicines Agency, amending Regulation (EC) No 1394/2007 and Regulation (EU) No 536/2014 and repealing Regulation (EC) No 726/2004, Regulation (EC) No 141/2000 and Regulation (EC) No 1901/2006 Proposal for a Directive of the European Parliament and of the Council on the Union code relating to medicinal products for human use, and repealing Directive 2001/83/EC and Directive 2009/35/EC - Exchange of views (179057/EU XXVII.GP)