Regulation (EU) 2023/1182 on specific rules relating to medicinal products for human use intended to be placed on the market in Northern Ireland figure dans le corpus Pharmaceuticals & Life Sciences parce que son titre officiel correspond à medicinal products. Source: EUR-Lex et dossier du Parlement européen; l'applicabilité à une entreprise dépend de ses activités. Methodology
Regulation (EU) 2023/1182 on specific rules relating to medicinal products for human use intended to be placed on the market in Northern Ireland: ce que cela signifie pour Pharmaceuticals & Life Sciences
Cette page explique en français pourquoi Regulation (EU) 2023/1182 on specific rules relating to medicinal products for human use intended to be placed on the market in Northern Ireland est lié à Pharmaceuticals & Life Sciences. La correspondance est fondée sur les termes officiels medicinal products; elle n'est pas un avis juridique.
- Acte
- 32023R1182
- Type
- règlement
- Étape
- Procedure completed
- Date
- 14 juin 2023
- Procédure
- 2023/0064(COD)
Ce que fait l'acte
PROPOSED ACT: Regulation of the European Parliament and of the Council. ROLE OF THE EUROPEAN PARLIAMENT: the European Parliament decides in accordance with the ordinary legislative procedure and on an equal footing with the Council. BACKGROUND: the Agreement on the withdrawal of the United Kingdom of Great Britain and Northern Ireland from the European Union entered into force on 1 February 2020. The Protocol on Ireland/Northern Ireland forms an integral part of the Withdrawal Agreement. The provisions of Union law listed in Annex 2 to the Protocol apply, under the conditions set out in that Annex, to and in the...
Pourquoi cela compte pour Pharmaceuticals & Life Sciences
Pharmaceutical and life-sciences companies face EU rules on medicines authorisation, clinical trials and supply-chain integrity across the single market. These are the EU acts most likely to apply.
Lex publie la connexion source entre le texte officiel et le secteur; l'impact précis dépend de l'entreprise, de ses produits et de ses marchés.
Autres textes dans le corpus Pharmaceuticals & Life Sciences
- Regulation (EU) 2022/839 laying down transitional rules for the packaging and labelling of veterinary medicinal products authorised or registered in accordance with Directive 2001/82/EC or Regulation (EC) No 726/200432022R0839
- Regulation (EU) 2022/123 on a reinforced role for the European Medicines Agency in crisis preparedness and management for medicinal products and medical devices32022R0123
- Regulation (EU) 2020/1043 on the conduct of clinical trials with and supply of medicinal products for human use containing or consisting of genetically modified organisms intended to treat or prevent coronavirus disease (COVID-19)32020R1043
Sources primaires
- Texte intégral sur EUR-Lex (32023R1182) ↗
- Dossier de procédure du Parlement européen (2023/0064(COD)) ↗
Données © Union européenne. Méthodologie.