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Proposal for a Regulation of the European Parliament and of the Council on establishing a framework of measures for strengthening Union's biotechnology and biomanufacturing sectors particularly in the area of health and amending Regulations (EC) No 178/2002, (EC) No 1394/2007, (EU) No 536/2014, (EU) 2019/6, (EU) 2024/795 and (EU) 2024/1938 (European Biotech Act)/Consolidated version of proposed amendments to the Biotech Act (Regulation) on clinical trials on medicinal products for human use (CTR) (Articles) (53363/EU XXVIII.GP)

EU-V: Arbeitsdokument

Proposal for a Regulation of the European Parliament and of the Council on establishing a framework of measures for strengthening Union's biotechnology and biomanufacturing sectors particularly in the area of health and amending Regulations (EC) No 178/2002, (EC) No 1394/2007, (EU) No 536/2014, (EU) 2019/6, (EU) 2024/795 and (EU) 2024/1938 (European Biotech Act)/Consolidated version of proposed amendments to the Biotech Act (Regulation) on clinical trials on medicinal products for human use (CTR) (Articles)

Gruppe: Gruppe "Arzneimittel und Medizinprodukte"

betrifft Sitzung am 14.01.2026

Erstellt am 13.01.2026

Eingelangt am 14.01.2026, CIxP Übermittlung

  • RAT: WK 480/26

Dokumente mit derselben Dokumentennummer als Basiszahl. Zusatzdokumente zur Änderung des Ausgangsdokuments werden hinzugefügt (COR, REV, ADD)
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Datum EU-Datenbanknr. Dokument der EU-Vorlage Sprache Einstufung
13.01.2026 53365/EU XXVIII.GP
  • RAT: WK 480/26 ADD 1
englisch LIMITE

Arbeitsdokument

Proposal for a Regulation of the European Parliament and of the Council on establishing a framework of measures for strengthening Union's biotechnology and biomanufacturing sectors particularly in the area of health and amending Regulations (EC) No 178/2002, (EC) No 1394/2007, (EU) No 536/2014, (EU) 2019/6, (EU) 2024/795 and (EU) 2024/1938 (European Biotech Act)/Consolidated version of proposed amendments to the Biotech Act (Regulation) on clinical trials on medicinal products for human use (CTR) (Annexes)

Eingelangt am 14.01.2026, CIxP Übermittlung
Dokumente, die sich auch auf die gegenständliche Sitzung (Gremium und Datum) beziehen.
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Datum Dok.Nr.
Dokumenten der EU-Institutionen zugeordnete, fortlaufende Nummer mit Jahreszahl, um diese eindeutig zu identifizieren.
Art Betreff
17.12.2025 RAT: 16919/25 EUST
EU-Vorlage: Offizielles Ratsdokument
Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices, and amending Regulation (EU) 2022/123 as regards the support of the European Medicines Agency for the expert panels on medical devices and Regulation (EU) 2024/1689 as regards the list of Union harmonisation legislation referred to in its Annex I (51578/EU XXVIII.GP)
21.12.2025 RAT: 16945/25 EUST
EU-Vorlage: Offizielles Ratsdokument
Proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL on establishing a framework of measures for strengthening Union's biotechnology and biomanufacturing sectors particularly in the area of health and amending Regulations (EC) No 178/2002, (EC) No 1394/2007, (EU) No 536/2014, (EU) 2019/6, (EU) 2024/795 and (EU) 2024/1938 (European Biotech Act) (52034/EU XXVIII.GP)
06.01.2026 RAT: WK 74/26 EUWK
Arbeitsdokument
Proposal for a Regulation of the European Parliament and of the Council amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices, and amending Regulation (EU) 2022/123 as regards the support of the European Medicines Agency for the expert panels on medical devices and Regulation (EU) 2024/1689 as regards the list of Union harmonisation legislation referred to in its Annex I/Consolidated version of proposed amendments to the MDR Regulation (Articles) (52571/EU XXVIII.GP)
06.01.2026 RAT: WK 79/26 EUWK
Arbeitsdokument
Proposal for a Regulation of the European Parliament and of the Council amending Regulations (EU) 2017/745 and (EU) 2017/746 as regards simplifying and reducing the burden of the rules on medical devices and in vitro diagnostic medical devices (IVDR), and amending Regulation (EU) 2022/123 as regards the support of the European Medicines Agency for the expert panels on medical devices and Regulation (EU) 2024/1689 as regards the list of Union harmonisation legislation referred to in its Annex I/Consolidated version of proposed amendments to the IVDR Regulation (Articles) (52572/EU XXVIII.GP)
06.01.2026 RAT: CM 5535/25 EUTO
EU-Vorlage Tagesordnung
Working Party on Pharmaceuticals and Medical Devices Date: 14 January 2026 Time: 10:00 Venue: COUNCIL JUSTUS LIPSIUS BUILDING Rue de la Loi 175, 1048 BRUSSELS (52593/EU XXVIII.GP)
11.01.2026 RAT: WK 341/26 EUWK
Arbeitsdokument
Flash from the Presidency for the Working Party on Pharmaceuticals and Medical Devices on 14 January 2026 (53136/EU XXVIII.GP)
13.01.2026 RAT: WK 345/26 EUWK
Arbeitsdokument
Presentation by the Commission on the Regulation to simplify rules on medical and in vitro daignostic devcies (53396/EU XXVIII.GP)
13.01.2026 RAT: WK 344/26 EUWK
Arbeitsdokument
Working Party on Pharmaceuticals and Medical Devices 14 January 2026 (53471/EU XXVIII.GP)
13.01.2026 RAT: WK 486/26 EUWK
Arbeitsdokument
Proposal for a Regulation of the European Parliament and of the Council on establishing a framework of measures for strengthening Union's biotechnology and biomanufacturing sectors particularly in the area of health and amending Regulations (EC) No 178/2002, (EC) No 1394/2007, (EU) No 536/2014, (EU) 2019/6, (EU) 2024/795 and (EU) 2024/1938 (European Biotech Act)/Consolidated version of proposed amendments to the Biotech Act (Regulation) on the Strategic Technologies for Europe Platform (STEP) (Articles) (53369/EU XXVIII.GP)
13.01.2026 RAT: WK 483/26 EUWK
Arbeitsdokument
Proposal for a Regulation of the European Parliament and of the Council on establishing a framework of measures for strengthening Union's biotechnology and biomanufacturing sectors particularly in the area of health and amending Regulations (EC) No 178/2002, (EC) No 1394/2007, (EU) No 536/2014, (EU) 2019/6, (EU) 2024/795 and (EU) 2024/1938 (European Biotech Act)/Consolidated version of proposed amendments to the Biotech Act (Regulation) on standards of quality and safety for substances of human origin intended for human application (Articles) (53366/EU XXVIII.GP)
13.01.2026 RAT: WK 485/26 EUWK
Arbeitsdokument
Proposal for a Regulation of the European Parliament and of the Council on establishing a framework of measures for strengthening Union's biotechnology and biomanufacturing sectors particularly in the area of health and amending Regulations (EC) No 178/2002, (EC) No 1394/2007, (EU) No 536/2014, (EU) 2019/6, (EU) 2024/795 and (EU) 2024/1938 (European Biotech Act)/Consolidated version of proposed amendments to the Biotech Act (Regulation) on General Food Law (Articles) (53370/EU XXVIII.GP)
13.01.2026 RAT: WK 484/26 EUWK
Arbeitsdokument
Proposal for a Regulation of the European Parliament and of the Council on establishing a framework of measures for strengthening Union's biotechnology and biomanufacturing sectors particularly in the area of health and amending Regulations (EC) No 178/2002, (EC) No 1394/2007, (EU) No 536/2014, (EU) 2019/6, (EU) 2024/795 and (EU) 2024/1938 (European Biotech Act)/Consolidated version of proposed amendments to the Biotech Act (Regulation) on veterinary medicinal products (Articles) (53367/EU XXVIII.GP)
13.01.2026 RAT: WK 482/26 EUWK
Arbeitsdokument
Proposal for a Regulation of the European Parliament and of the Council on establishing a framework of measures for strengthening Union's biotechnology and biomanufacturing sectors particularly in the area of health and amending Regulations (EC) No 178/2002, (EC) No 1394/2007, (EU) No 536/2014, (EU) 2019/6, (EU) 2024/795 and (EU) 2024/1938 (European Biotech Act)/Consolidated version of proposed amendments to the Biotech Act (Regulation) on advanced therapy medicinal products (Articles) (53364/EU XXVIII.GP)
13.01.2026 RAT: WK 468/26 EUWK
Arbeitsdokument
Report on Cybersecurity of connected medical devices – where we are and what’s next/Presentation (53460/EU XXVIII.GP)
Gesetzgebungsvorhaben der Kommission erhalten eine fortlaufende Nummer mit Jahresangabe und Kürzel des Verfahrens (z.B.: COD, NLE). Diese Zahl wird von den beteiligten EU-Institutionen über sämtliche Etappen eines Verfahrens bis zur Annahme verwendet. Dies ermöglicht die Zusammenstellung vollständiger Dossiers
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Interinstitutionelle Zahl
Der Link führt zu den einzelnen Dokumenten dieses Vorhabens.
Link
2025/0406 COD Legislative Observatory
Zusätzliche Dokumente, auf die im Text Bezug genommen oder verwiesen wird (Vordokumente und sonstige Verweise)
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Mit den Sachgebietscodes werden die in einem Dokument behandelten Themenbereiche des Rates ausgewiesen. Der Link führt zu Dokumenten mit dem gleichen Sachgebiet
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Dieser Link führt zum Filter für die Dokumentenauswahl nach übergeordneten Themen
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