SANT - Public Health

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)

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

Amending Directives 2001/18/EC and 2010/53/EU as regards the placing on the market of genetically modified micro-organisms and the processing of organs

Guidelines for the 2027 Budget - Section III

Modernised rules for patients’ rights in cross-border healthcare

Establishing the European Fund for economic, social and territorial cohesion, agriculture and rural, fisheries and maritime, prosperity and security for the period 2028-2034

Discharge 2024: General budget of the EU - Joint Undertakings

Discharge 2024: General budget of the EU - European Parliament

Discharge 2024: General budget of the EU - Court of Justice of the European Union

Discharge 2024: General budget of the EU - European Economic and Social Committee

Discharge 2024: General budget of the EU - Court of Auditors

Discharge 2024: General budget of the EU - European Council and Council

Discharge 2024: General budget of the EU - Agencies

Discharge 2024: General budget of the EU - Commission

Discharge 2024: General budget of the EU - European Ombudsman

Discharge 2024: General budget of the EU - Committee of the Regions

Commission Delegated Regulation amending Delegated Regulation (EU) 2023/2197 as regards the date of application

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

Revises EU rules on the authorisation and supervision of medicinal products and updates the framework for the European Medicines Agency.

Union code relating to medicinal products for human use, and repealing Directive 2001/83/EC and Directive 2009/35/EC

Revises the EU pharmaceutical framework to improve access to medicines, incentivise innovation, and strengthen supply security.