The Greek Patients’ Association is committed to asserting the rights of the chronically ill through coherent actions and determined efforts. Through letters to institutions and representatives, the Association demonstrates the importance of open communication in addressing issues that affect the lives of patients.
The advocacy actions reflect the Association’s determination to positively influence the legislative and policy environment for the benefit of chronically ill patients. At every step, the Association remains at the side of patients, fighting for justice and equity in healthcare
- Committee for Control and Advertising of EOF (National Organization for Medicines)
- Ethics Committee for Clinical Trials
- Monitoring Committee for Pharmaceutical Expenditure, Therapeutic Protocols, and Patient Registries
- Expert Committee for Public Health
- National Committee for Rare Diseases
- Committee for the Protection of the Rights of Healthcare Service Recipients
- Committee for Monitoring Drug Shortages
- Research and Technology Committee of the Central Health Council (KESY)
- National Committee for the Development of Palliative Care
- Working Group for the Development of Clinical Trials and Biomedical Research in the Country
- Board of Directors of the “National Center for Health Quality Assessment and Technology S.A. (EKAPY S.A.)
- Health Services Evaluation Committee
- Working Group for the Reconstruction of EOPYY (National Organization for the Provision of Health Services)
- National Ethics Committee for Clinical Trials
- Committee for the Modernization of the Institutional Framework and Implementation of Involuntary Hospitalization
- Special Oversight Committee for the Protection of the Rights of Individuals with Mental Disorders
- Committee for Examining the Need to Create Patient Registries
- Scientific Working Group for the Development and Periodic Update of the National Registry for Rare Diseases