Apply for the EURORDIS Summer School 2018!
Patients are taking on ever increasing roles in advocating for medicines development, equal access to treatments across Europe and ensuring that medical information is clear, accurate and comprehensible. In order to help prepare them for these roles and as part of its commitment to empowering people living with rare diseases, EURORDIS launched its own training programme for expert patients in 2008.
The programme allows patients and researchers to sharpen their advocacy skills and gain an understanding of the regulatory process of orphan medicinal products so that they are able to advocate at a European level.
The programme has online and face-to-face components. The face-to-face portion trains 40 expert patients annually as part of an intensive 4.5-day course held in Barcelona, Spain.
The next edition of the EURORDIS Summer School will take place in 11 - 15 June 2018 in Barcelona.
The application process will open on 16 October 2017. Details on how to apply will be posted on this page.
If you have any questions regarding the EURORDIS Summer School please contact Nancy Hamilton email@example.com.
How to apply
The next edition of the EURORDIS Summer School will take place in June 11 - 15 2018 in Barcelona. The application process will open on 16 October 2017. Details on how to apply will be posted on this page. For more information about EURORDIS Summer School please contact Nancy Hamilton firstname.lastname@example.org.
Content of the programme
The EURORDIS Summer School covers the follow topics:
- Clinical Trials Methodology
- Clinical Research
- Ethical Considerations in Medicines Development
- Regulatory affairs
- Health Technology Assessment
- Marketing Authorisations
Why the Summer School was developed
The Summer School was developed to fill specific needs identified by expert patients, EURORDIS and the European Medicines Agency. Expert patients from EURORDIS are permanent representatives on EMA Scientific Committees and working parties. EURORDIS recognises their need for support and training that includes an overview of clinical research and methodology, medicines development and regulatory procedures.
In 2000, the Committee for Orphan Medicinal Products (COMP) was formed at the European Medicines Agency (EMA) and the European authorities had the foresight to include patients' representatives as permanent and full members with equal voting rights. Three patients' representatives sit on this committee and the position of Vice-Chair of the COMP has to date always been held by a patients' representative.
Since this time, a working party and three more scientific committees have been created, all of which include patients' representatives:
- Patients' and Consumers' Working Party (PCWP) in 2006
- Paediatric Committee (PDCO) in 2008
- Committee for Advanced Therapies (CAT) in 2009
- Pharmacovigilance and Risk Assessment Committee (PRAC) in 2012
Expert Patients are also frequently solicited for their input on the development of specific products for their disease, e.g.; via the process of Protocol Assistance with the Scientific Advice Working Party (SAWP).
To date, the Summer School has trained over 400 participants from more than 40 countries and representing over 70 different diseases. Summer School alumni report an increased awareness of the importance of their involvement in all aspects of medicines development and of their potential to be a real force. Participants also recognise the need for patients' organisations to collaborate internationally as well as the importance of involvement in the activities of the European Medicines Agency (EMA) and EURORDIS. The training experience reinforces participants' sense of community, and increases their individual capacities.
Ahead of the Summer School in Barcelona, participants are invited to take part in a pre-training course. In addition to the face-to-face training programme, trainees have access to freely available online modules, webcasts and slide presentations to allow them to prepare for the face-to-face training and to review and refer back to the content once they have completed the training.