| Written submissions and meetings with stakeholder organisations. | Kanser
> Kanser: çoğu türü | Düzenleyici ortaklık
> Düzenleyici kurumlarla çalışma | We do not communicate with patients directly | National | Regularly | 115055433125 |
| The Hellenic League Against Rheumatism (ELEANA) regularly represents patient interests to national and European regulators through formal consultations, written submissions, participation in policy dialogues, and involvement in European patient advocacy platforms (e.g., EULAR [European Alliance of Associations for Rheumatology] PARE [People with Arthritis/Rheumatism in Europe], EPF [European Patients' Forum], GAfPA [Global Alliance for Patient Access]). | Romatizmal
> Romatizmal hastalıklar: çoğu tür | Düzenleyici ortaklık
> Politika yapıcılar/düzenleyicilerle toplantılara katılın/kolaylaştırın | 100.000 | National | Regularly | 119025688550 |
| As a member of secondary and tertiary federations representing persons with disabilities and persons with multiple sclerosis, and through our direct engagement with the state, we advocate on behalf of our members. | Nörolojik
> Multipl skleroz | Düzenleyici ortaklık
> Diğer sağlık savunucularıyla | 1.000 | Regional | Regularly | 115007075579 |
| Submits proposals to the collective "umbrella" body. | Nadir
> Nadir hastalıklar: çoğu tür | Düzenleyici ortaklık
> Diğer sağlık savunucularıyla | 1.000 | National | Sometimes | 115019806061 |
| Through written submissions to the Ministry, engagement with local Members of Parliament, direct interpersonal contacts, and the Patient Association of Greece. | Nörodejeneratif
> Alzheimer | Düzenleyici ortaklık
> Diğer sağlık savunucularıyla | 1.000 | Regional | Regularly | 115049818475 |
| Through ΕΛΟΔΙ [Ελληνική Ομοσπονδία για τον Διαβήτη - Hellenic Federation for Diabetes]. | Endokrin
> Diyabet (hem tip 1 hem de tip 2) | Düzenleyici ortaklık
> Diğer sağlık savunucularıyla | 100 | Regional | Sometimes | 115060878962 |
| The Hellenic League Against Rheumatism (ELEANA) regularly represents patient interests to national and European regulators through formal consultations, written submissions, participation in policy dialogues, and involvement in European patient advocacy platforms (e.g., EULAR [European Alliance of Associations for Rheumatology] PARE [People with Arthritis/Rheumatism in Europe], EPF [European Patients' Forum], GAfPA [Global Alliance for Patient Access]). | Romatizmal
> Romatizmal hastalıklar: çoğu tür | Düzenleyici ortaklık
> Diğer sağlık savunucularıyla | 100.000 | National | Regularly | 119025688550 |
| AGORA Federation represents patient perspectives through EU-level policy dialogues and consultations, and via participation in European patient advocacy platforms. We contribute input on access, reimbursement, unmet needs, and quality of life across rheumatic and musculoskeletal diseases from a cross-country (Southern Europe) perspective. | Romatizmal
> Romatizmal hastalıklar: çoğu tür | Düzenleyici ortaklık
> Diğer sağlık savunucularıyla | We do not communicate with patients directly | International | Rarely | 119025711207 |
| Advocacy for patient pharmacotherapy at the Ministry of Health. | Kemik
> Osteoporoz | Politika ve mevzuatı etkileme
> Sağlık politikası ve mevzuatını etkileme | 10.000 | National | Sometimes | 114996725641 |
| National Strategic Plan for CVD [Cardiovascular Disease]. | Kardiyovasküler
> Kardiyovasküler: çoğu tür | Politika ve mevzuatı etkileme
> Sağlık politikası ve mevzuatını etkileme | 1.000 | National | Rarely | 115006858228 |
| As a member of secondary and tertiary federations representing persons with disabilities and persons with Multiple Sclerosis, and through direct engagement with public authorities, we advocate on behalf of our members by submitting requests for access to therapeutic treatments and therapies, as well as for the protection of their rights vis-à-vis the state. | Nörolojik
> Multipl skleroz | Politika ve mevzuatı etkileme
> Sağlık politikası ve mevzuatını etkileme | 1.000 | Regional | Regularly | 115007075579 |
| We engage in lobbying activities to advance and protect the interests of patients. | Bakıcılar
> Bakıcılar, aile, arkadaşlar | Politika ve mevzuatı etkileme
> Sağlık politikası ve mevzuatını etkileme | 100 | National | Rarely | 115047040745 |
| Where consultation processes are available on the relevant websites, we submit our positions, and we also direct formal requests to the Ministries of Health and Labour [in Greece]. | Nörolojik
> Multipl skleroz | Politika ve mevzuatı etkileme
> Sağlık politikası ve mevzuatını etkileme | 1.000 | Regional | Rarely | 115049438439 |
| Through written submissions to the Ministry, engagement with local Members of Parliament, direct interpersonal contacts, and the Patient Association of Greece. | Nörodejeneratif
> Alzheimer | Politika ve mevzuatı etkileme
> Sağlık politikası ve mevzuatını etkileme | 1.000 | Regional | Regularly | 115049818475 |
| Wherever public consultations are hosted on the relevant websites, we submit our views. | Nörolojik
> Multipl skleroz | Politika ve mevzuatı etkileme
> Kamuoyu dinlemelerine ve istişarelere katılın | 1.000 | Regional | Rarely | 115049438439 |
| Where consultation processes are available on the relevant websites, we submit our positions, and we also direct formal requests to the Ministries of Health and Labour [in Greece]. | Nörolojik
> Multipl skleroz | Politika ve mevzuatı etkileme
> Kamuoyu dinlemelerine ve istişarelere katılın | 1.000 | Regional | Rarely | 115049438439 |
| AGORA Federation represents patient perspectives through EU-level policy dialogues and consultations, and via participation in European patient advocacy platforms. We contribute input on access, reimbursement, unmet needs, and quality of life across rheumatic and musculoskeletal diseases from a cross-country (Southern Europe) perspective. | Romatizmal
> Romatizmal hastalıklar: çoğu tür | Politika ve mevzuatı etkileme
> Kamuoyu dinlemelerine ve istişarelere katılın | We do not communicate with patients directly | International | Rarely | 119025711207 |
| Through written submissions to the Ministry, engagement with local Members of Parliament, direct interpersonal contacts, and the Patient Association of Greece. | Nörodejeneratif
> Alzheimer | Politika ve mevzuatı etkileme
> Parlamenterleri ve siyasi liderleri harekete geçirin | 1.000 | Regional | Regularly | 115049818475 |
| AGORA Federation represents patient perspectives through EU-level policy dialogues and consultations, and via participation in European patient advocacy platforms. We contribute input on access, reimbursement, unmet needs, and quality of life across rheumatic and musculoskeletal diseases from a cross-country (Southern Europe) perspective. | Romatizmal
> Romatizmal hastalıklar: çoğu tür | Fiyatlandırma ve erişilebilirlik savunuculuğu
> Adil ilaç fiyatlandırması için savunuculuk yapın | We do not communicate with patients directly | International | Rarely | 119025711207 |
| Advocacy for patient pharmacotherapy at the Ministry of Health. | Kemik
> Osteoporoz | Erişim yollarının iyileştirilmesi
> İlaçlara/sağlık hizmetlerine eşit erişimi kolaylaştırma | 10.000 | National | Sometimes | 114996725641 |
| Advocacy for access to medicines, diagnostic tests, and related services. | Nadir
> Von Hippel-Lindau sendromu | Erişim yollarının iyileştirilmesi
> İlaçlara/sağlık hizmetlerine eşit erişimi kolaylaştırma | 100 | National | Regularly | 115006788497 |
| Advocacy for access to medicines, diagnostic tests, and related services. | Nadir
> Von Hippel-Lindau sendromu | Erişim yollarının iyileştirilmesi
> İlaçlara/sağlık hizmetlerine eşit erişimi kolaylaştırma | 100 | National | Regularly | 115006788497 |
| As a member of secondary and tertiary federations representing persons with disabilities and persons with multiple sclerosis, and through direct engagement with public authorities, we advocate on behalf of our members by submitting requests for access to therapeutic treatments and therapies, as well as for the protection of their rights vis-à-vis the state. | Nörolojik
> Multipl skleroz | Erişim yollarının iyileştirilmesi
> İlaçlara/sağlık hizmetlerine eşit erişimi kolaylaştırma | 1.000 | Regional | Regularly | 115007075579 |
| Issues relating to employment, accessibility, health inequalities, and the management of treatment options. | Kanser
> Kanser: çoğu türü | Erişim yollarının iyileştirilmesi
> İlaçlara/sağlık hizmetlerine eşit erişimi kolaylaştırma | 1.000 | National | Regularly | 115058727551 |
| … The Hellenic League Against Rheumatism (ELEANA) contributes patient perspectives on access to treatments, reimbursement, unmet needs, and quality of life in autoimmune rheumatic diseases, both at national level (Greece) and at EU level. | Romatizmal
> Romatizmal hastalıklar: çoğu tür | Erişim yollarının iyileştirilmesi
> İlaçlara/sağlık hizmetlerine eşit erişimi kolaylaştırma | 100.000 | National | Regularly | 119025688550 |
| AGORA Federation represents patient perspectives through EU-level policy dialogues and consultations, and via participation in European patient advocacy platforms. We contribute input on access, reimbursement, unmet needs, and quality of life across rheumatic and musculoskeletal diseases from a cross-country (Southern Europe) perspective. | Romatizmal
> Romatizmal hastalıklar: çoğu tür | Erişim yollarının iyileştirilmesi
> İlaçlara/sağlık hizmetlerine eşit erişimi kolaylaştırma | We do not communicate with patients directly | International | Rarely | 119025711207 |
| … The Hellenic League Against Rheumatism (ELEANA) contributes patient perspectives on access to treatments, reimbursement, unmet needs, and quality of life in autoimmune rheumatic diseases, both at national level (Greece) and at EU level. | Romatizmal
> Romatizmal hastalıklar: çoğu tür | Kanıta dayalı hasta girdisi
> Kararları bilgilendirmek için hasta içgörülerini kullanın | 100.000 | National | Regularly | 119025688550 |
| AGORA Federation represents patient perspectives through EU-level policy dialogues and consultations, and via participation in European patient advocacy platforms. We contribute input on access, reimbursement, unmet needs, and quality of life across rheumatic and musculoskeletal diseases from a cross-country (Southern Europe) perspective. | Romatizmal
> Romatizmal hastalıklar: çoğu tür | Kanıta dayalı hasta girdisi
> Kararları bilgilendirmek için hasta içgörülerini kullanın | We do not communicate with patients directly | International | Rarely | 119025711207 |
| Patient interests only [to drug regulatory authorities]. | Bağışık
> Primer immün yetmezlikler | Kanıta dayalı hasta girdisi
> Hasta hikayelerinden ve yaşanmış deneyim anlatılarından yararlanın | 100 | Regional | Sometimes | 115055418373 |
| Advocacy for access to medicines, diagnostic tests, and related services. | Nadir
> Von Hippel-Lindau sendromu | Tanı ve ilaç teslimatı
> Tarama ve erken teşhisi destekleyin | 100 | National | Regularly | 115006788497 |
| Participation in Ministry committees addressing chronic disease patients, medicinal products, patient rights. | Belirtilmemiş
> Belirtilmemiş | Kurumsal yönetişim
> Hükümet danışma organlarında temsili sağlayın | 1.000 | National | Rarely | 115060548215 |
| As a member of secondary and tertiary federations representing persons with disabilities and persons with Multiple Sclerosis, and through direct engagement with public authorities, we advocate on behalf of our members by submitting requests for access to therapeutic treatments and therapies, as well as for the protection of their rights vis-à-vis the state. | Nörolojik
> Multipl skleroz | Hasta haklarını koruma/yaşam kalitesini iyileştirme
> Hasta deneyimini koruma/iyileştirme | 1.000 | Regional | Regularly | 115007075579 |
| As a member of secondary and tertiary federations representing persons with disabilities and persons with multiple sclerosis, and through direct engagement with public authorities, we advocate on behalf of our members by submitting requests for access to therapeutic treatments and therapies, as well as for the protection of their rights vis-à-vis the state. | Nörolojik
> Multipl skleroz | Hasta haklarını koruma/yaşam kalitesini iyileştirme
> Hasta deneyimini koruma/iyileştirme | 1.000 | Regional | Regularly | 115007075579 |
| Issues relating to employment, accessibility, health inequalities, and the management of treatment options. | Kanser
> Kanser: çoğu türü | Hasta haklarını koruma/yaşam kalitesini iyileştirme
> Hasta deneyimini koruma/iyileştirme | 1.000 | National | Regularly | 115058727551 |
| Advocating for quality of care and quality of life for patients. | Kanser
> Kanser: meme | Hasta haklarını koruma/yaşam kalitesini iyileştirme
> Yaşam kalitesine vurgu yapılmasının teşvik edilmesi | 5.000 | National | Regularly | 115019649379 |
| Advocating for quality of care and quality of life for patients. | Kanser
> Kanser: meme | Hasta haklarını koruma/yaşam kalitesini iyileştirme
> Yaşam kalitesine vurgu yapılmasının teşvik edilmesi | 5.000 | National | Regularly | 115019649379 |
| Issues relating to employment, accessibility, health inequalities, and the management of treatment options. | Kanser
> Kanser: çoğu türü | Hasta haklarını koruma/yaşam kalitesini iyileştirme
> Yaşam kalitesine vurgu yapılmasının teşvik edilmesi | 1.000 | National | Regularly | 115058727551 |
| AGORA Federation represents patient perspectives through EU-level policy dialogues and consultations, and via participation in European patient advocacy platforms. We contribute input on access, reimbursement, unmet needs, and quality of life across rheumatic and musculoskeletal diseases from a cross-country (Southern Europe) perspective. | Romatizmal
> Romatizmal hastalıklar: çoğu tür | Hasta haklarını koruma/yaşam kalitesini iyileştirme
> Yaşam kalitesine vurgu yapılmasının teşvik edilmesi | We do not communicate with patients directly | International | Rarely | 119025711207 |
etkileşimler
eylemler & savunuculuk
8 bahsetmeler
