Subject "4.20.02 Medical research"

Dossiers (26)

EEA Agreement: amending Protocol 31 on cooperation in specific fields outside the four freedoms (EU4Health Programme). EU position
Preparedness for COVID-19 vaccination strategies and vaccine deployment
Labelling requirements for unauthorised investigational and unauthorised auxiliary medicinal products for human use
Standards of quality and safety for substances of human origin intended for human application
Resolution on EU transparency in the development, purchase and distribution of COVID-19 vaccines
Derogation from certain obligations concerning investigational medicinal products made available in the United Kingdom with respect to Northern Ireland as well as in Cyprus, Ireland and Malta
Programme for the Union's action in the field of health for the period 2021-2027 (“EU4Health Programme”)
European One Health action plan against antimicrobial resistance (AMR)
Promoting gender equality in mental health and clinical research
eHealth Action Plan 2012-2020 - Innovative healthcare for the 21st century
Declaration on children with Down syndrome
Microbial challenge - rising threats from antimicrobial resistance
Clinical trials on medicinal products for human use
Voluntary and unpaid donation of tissues and cells
Third programme for the Union's action in the field of health (2014-2020)
Resolution on the Tuberculosis Vaccine Initiative (TBVI) - practical implementation of the Europe 2020 strategy with a view to meeting MDG 6 and eliminating tuberculosis by 2050
European initiative on Alzheimer’s disease and other dementias
Resolution on Joint Programming of research to combat neurodegenerative diseases, in particular Alzheimer's disease
Joint programming of research activities: measures to combat neurodegenerative diseases, in particular Alzheimer's
Medical devices and active implantable medical devices
Life sciences and biotechnology: a strategy for Europe
Human tissues and cells: quality and safety for the donation, procurement, testing, processing, preservation, storage and distribution
Health implications of the Directive 93/42/EEC of 14 June 1993 on medical devices
Orphan medicinal products
In vitro diagnostic medical devices: security requirements
Specific research programme RTD: biomedicine and health (1994-1998)