Health legislation and policy

European Health Data Space

Critical Medicines Act

Patients' rights in cross-border healthcare

Programme for the Union's action in the field of health for the period 2021-2027 (“EU4Health Programme”)

Medical devices

European Medicines Agency

Standards of quality and safety for substances of human origin intended for human application

European One Health action plan against antimicrobial resistance (AMR)

Health technology assessment

In vitro diagnostic medical devices

Reducing health inequalities in the EU

Basic safety standards for protection against the dangers arising from exposure to ionising radiation

Third programme for the Union's action in the field of health (2014-2020)

Asbestos related occupational health threats and prospects for abolishing all existing asbestos

Standards of quality and safety of human organs intended for transplantation

Implementation report on Regulation (EC) No1924/2006 on nutrition and health claims made on foods

Health rules: animal by-products and derived products not intended for human consumption

Action against cancer: European partnership

Green Paper on the role of civil society in drugs policy in the EU

Medicinal products for human use: pharmacovigilance of products

Voluntary and unpaid donation of tissues and cells

Supplementary protection certificate for medicinal products. Recast

Protection of vulnerable adults

Cosmetic products. Recast. "Cosmetics Regulation"

Together for health: a strategic approach for the EU 2008-2013

Medicinal products for human and veterinary use

Action plan on organ donation and transplantation (2009-2015): strengthened cooperation between Member States

Organ donation and transplantation: policy actions at EU level

Medicinal products for human and veterinary use: marketing authorisations

Animal health requirements: non-commercial movement of pet animals