Draft proposal for a Regulation 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)/Comments from Austria and other Member States on clinical trials in Article 58 and Annex II (86012/EU XXVIII.GP)

RAT: WK 10994/26 LIMITE
28.07.2026
englisch

Erklärung Österreichs

Draft proposal for a Regulation 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)/Comments from Austria and other Member States on clinical trials in Article 58 and Annex II

Gruppe: Gruppe "Arzneimittel und Medizinprodukte"

betrifft Sitzungen am 22.07.2026 und 23.07.2026

Erstellt am 28.07.2026

Eingelangt am 29.07.2026, CIxP Übermittlung

 
Datum EU-Datenbanknr. Dokument der EU-Vorlage Sprache Einstufung
29.07.2026 86092/EU XXVIII.GP
englisch LIMITE

Arbeitsdokument

Draft proposal for a Regulation 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)/Comments from Hungary and Sweden on clinical trials in Article 58 and Annex II

Eingelangt am 30.07.2026, CIxP Übermittlung

30.07.2026 86215/EU XXVIII.GP
englisch LIMITE

Arbeitsdokument

Draft proposal for a Regulation 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)/Additional comments from Germany and Poland

Eingelangt am 31.07.2026, CIxP Übermittlung

30.08.2026 89183/EU XXVIII.GP
englisch LIMITE

Arbeitsdokument

Draft proposal for a Regulation 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)/Comments from Greece and Luxembourg on clinical trials in Article 58 and Annex II

Eingelangt am 31.08.2026, CIxP Übermittlung

 
Datum Dok.Nr.
Art Betreff
09.07.2026 RAT: CM 3652/26 EUTO
Working Party on Pharmaceuticals and Medical Devices Date: 22 and 23 July 2026 Time: 10:00, 10:00 Venue: COUNCIL LEX BUILDING Rue de la Loi 145, 1048 BRUSSELS (83493/EU XXVIII.GP)
09.07.2026 RAT: CM 3652/26 EUTO
Working Party on Pharmaceuticals and Medical Devices Date: 22 and 23 July 2026 Time: 10:00, 10:00 Venue: COUNCIL LEX BUILDING Rue de la Loi 145, 1048 BRUSSELS (83493/EU XXVIII.GP)
12.07.2026 RAT: WK 10325/26 EUWK
Presidency Flash for the meeting of the Working Party on Pharmaceuticals and Medical Devices on 22 and 23 July 2026 (83714/EU XXVIII.GP)
12.07.2026 RAT: WK 10325/26 EUWK
Presidency Flash for the meeting of the Working Party on Pharmaceuticals and Medical Devices on 22 and 23 July 2026 (83714/EU XXVIII.GP)
21.07.2026 RAT: WK 10846/26 EUWK
Draft proposal for a Regulation 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)/Presentation by the Commission on Clinical Trial Regulation revision (85206/EU XXVIII.GP)
21.07.2026 RAT: WK 10846/26 EUWK
Draft proposal for a Regulation 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)/Presentation by the Commission on Clinical Trial Regulation revision (85206/EU XXVIII.GP)
 
 
Interinstitutionelle Zahl
Link
2025/0406 COD