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Working Party on Pharmaceuticals and Medical Devices Date: 29 and 30 January 2025 Time: 10:00, 10:00 Venue: COUNCIL JUSTUS LIPSIUS BUILDING Rue de la Loi 175, 1048 BRUSSELS (9297/EU XXVIII.GP)

EU-V: Tagesordnung

Working Party on Pharmaceuticals and Medical Devices Date: 29 and 30 January 2025 Time: 10:00, 10:00 Venue: COUNCIL JUSTUS LIPSIUS BUILDING Rue de la Loi 175, 1048 BRUSSELS

Gruppe: Gruppe "Arzneimittel und Medizinprodukte"

betrifft Sitzungen am 29.01.2025 und 30.01.2025

Erstellt am 23.01.2025 von: Gesundheit

Eingelangt am 23.01.2025, U32 Übermittlung

RAT: CM 1271/25
PDF

Linkart	Link
RAT Rat	5475/25
RAT Rat	5539/25
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
23.01.2025	RAT: 5539/25	EUST EU-Vorlage: Offizielles Ratsdokument	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 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 - Exchange of views (9296/EU XXVIII.GP)
23.01.2025	RAT: 5539/25	EUST EU-Vorlage: Offizielles Ratsdokument	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 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 - Exchange of views (9296/EU XXVIII.GP)
23.01.2025	RAT: 5475/25	EUST EU-Vorlage: Offizielles Ratsdokument	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 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 - Exchange of views (9288/EU XXVIII.GP)

Dok.Nr.

Betreff

RAT: 5539/25

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 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 - Exchange of views (9296/EU XXVIII.GP)

RAT: 5475/25

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 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 - Exchange of views (9288/EU XXVIII.GP)