XII EUROPEAN PATIENTS’ RIGHTS DAY 2018 at European Parliament (23 May 2018)

From the therapeutic adherence to the therapeutic alliance: improving trust between patients and professionals to increase healthcare outcomes.

Europe and the Member States have a duty to attempt any possible solution to increase the level of adherence to treatment, in order to achieve important savings and improve the quality of life of citizens. This could be confirmed, of course, also in the next mandate of the EU Institutions. This is, in synthesis, the main message coming from the 12th edition of the European Patients’ Rights Day, held at the European Parliament in Brussels today, and organized by Active Citizenship Network, the European Branch of the Italian NGO Cittadinanzattiva.

The event was hosted by MEP David Borrelli, introduced by a video message of the European Commissioner for Health and Food Safety Andriukaitis, and realized thanks the support of: MSD, Merck, Bayer, Boehringer Ingelheim, GAfPA.



Italy Flag 16

A way to make visible the invisible on chronic pain through the arts

 "ARTISTS AGAINST PAIN" is the title of the cultural event scheduled for next March 17 in Milan, Italy, aimed to unit arts and advocacy groups on the topic of chronic pain.

The initiative is promoted by the artistic cultural association “Bioforme” in partnership with the European branch of the Italian NGO Cittadinanzattiva, Active Citizenship Network, the Maltese association "No Pain Foundation", and the patronage of Municipality 8 of the City of Milan.


European Commission recognises Societal Impact of Pain (09 June 2017)

Martin Seychell, Deputy Director General Dg Sante, Formally Announces Launch of Pain Expert and Stakeholder Group on the Eu Health Policy Platform at the Societal Impact of Pain Symposium

Valletta, Malta, June 9, 2017. The 7th annual Societal Impact of Pain (SIP) symposium comes to an end today, with clear policy recommendations having been formulated to change pain care in the European Union for the better and alleviate the effect of pain on society. Martin Seychell, Deputy Director General in the Health and Food Safety's Directorate, announced in a speech that the European Commission is following SIP’s lead and has launched the EU Health Policy Platform to build a bridge between health systems and policy makers. Among other health policy areas, the societal impact of pain is included as well and will have a dedicated expert group.


Chronic pain is included in the Council conclusions during the Maltese Presidency (19 June 2017)

A major step forward for pain patients! Health ministers call for action on access to treatment for patients suffering from chronic pain

Friday June 16th, at a high level EU meeting, Health Ministers included chronic pain in the conclusions inviting Member States to evaluate access to treatment.  

Brussels, Belgium – Friday June 16th, the Council of the European Union on Employment, Social Policy, Health and Consumer Affairs adopted its conclusions on “Encouraging Member States-driven Voluntary Cooperation of Health Systems” (1).



How to better access to innovative therapies: in Brussels today the
11th Patients’ Rights Day promoted by Active Citizenship Network and dozens of European civic associations.

Active Citizenship Network is celebrating today, with a multi-stakeholder conference at EESC in Brussels the 11th European Patients’ Rights Day.
The aim of the convention was to discuss, inform and suggest new approaches to the existing European and National Medicines Regulatory Systems, for better management of access to innovation. Indeed, the access to innovative therapies strongly contributes to define the quality of life of patients and the quality of healthcare services provided, respecting the fundamental values recognised by the European Charter of Patients’ Rights, promoted by Active Citizenship Network in 2012, and undersigned by dozens of European civic associations (list available on www.activecitizenship.net). The event was an occasion to inform, discuss and take commitments to improve the respect of patients’ rights and their involvement in the policy-making and regulatory processes at national and European level.



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