contadores web
  • Contact

ExPRESS 2015 Expert Patient and Researcher EURORDIS Summer School

The 2015 version of the Summer School will be held from 1-5 June, 2015  in Barcelona, Spain. Expert patient representatives, researchers and trainers from patient organisations, research institutes and the European Medicines Agency will join together.

The 2015 version of the Summer School will be held from 1-5 June, 2015  in Barcelona, Spain. Expert patient representatives, researchers and trainers from patient organisations, research institutes and the European Medicines Agency will join together to take part in a new version of the Summer School called “ExPRESS 2015”, which stands for Expert Patients and Researchers EURORDIS Summer School.

Below you will find links to the Message for applicants, the Programme, and the  Application form. Please note that the deadline is 8 December, 2014.

punto verde


punto verde  Application form
punto verde  Letter for applicants
punto verde  Highlights of the Seventh EURORDIS Summer School

The Summer School is an annual initiative created by EURORDIS in 2008 and financed by the:

punto verde

2008 to 2010 DIA Philanthropy Programme 

punto verde 

2008 to 2015 French Muscular Dystrophy Association (AFM)

punto verde 

2008 to 2015 Inserm

punto verde 

2008 to 2015 Fundació Doctor Robert UAB

punto verde 

2008 to 2015 Executive Agency for Health and Consumers (EAHC) Operating Grant

punto verde 

2012 to 2015 European Clinical Research Infrastructure Network (ECRIN)

punto verde 

2013 to 2015 Platforma Malalties Minoritaries

punto verde

2015 Cost Action Exon Skipping BM1207


The EURORDIS Summer School trains patients' advocates in the areas of :

 punto verde

Clinical Trials Methodology

 punto verde

Statistics in Clinical Research

 punto verde

Ethical Considerations in Medicines Development

 punto verde

Regulatory affairs

 punto verde

Health Technology Assessment

 punto verde

Marketing Authorisations


This training builds participants' capacities to act as experts in regulatory processes and further their implication in medicines development and advocacy actions both at the national and European levels. 


An annual event in Barcelona

Every year the Summer School is held in Barcelona, Spain, and to date has welcomed over 227 participants from more than 30 countries and representing over 70 different diseases. The EURORDIS Summer School is organised in collaboration with the Platforma Malaties Minoritaries and Professor Josep Torrent i Farnell and his team at the Universidad Autonoma de Barcelona. 

Participants are selected by an ad hoc committee according to their level of English language skills, their advocacy experience, and their willingness to be involved in medicines development and regulatory affairs at the European level.

In this unique training course tailored for EU patients' representatives, the material is developed and presented by experts from academia, regulatory agencies and patients' advocates, with extensive experience in their field. 


Positive results, greater understanding, further involvement

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.

Freely available on-line modules extend the content of the Summer School by providing recordings of all presentations and an e-learning tool  in clinical trial methodology, statistics and ethics. 


The EMA and Summer School

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:

punto verde Patients' and Consumers' Working Party (PCWP) (2006)
punto verde

Paediatric Committee (PDCO) in 2008

punto verde

Committee for Advanced Therapies (CAT) in 2009

punto verde

Pharmacovigilance and Risk Assessment Committee (PRAC) in 2012


Patients' representatives are also frequently solicited as experts 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).

In addition to these regulatory activities, patients' representatives are involved in:

punto verde

Advocating for medicines development

punto verde

Ensuring clear information for patients

punto verde

Attempting to achieve equal access to treatments both at European and national levels


EURORDIS, which has permanent representatives in the EMA Scientific Committees (COMP, PDCO, CAT and working parties) recognised a need to provide support to these patients' advocates. A training course providing an overview of clinical trials, medicines development and regulatory procedures was identified as an essential tool to address these needs - hence the EURORDIS Summer School was born.

For more information about EURORDIS Summer School please contact Nancy Hamilton




Avda. Barcelona nÂș 174 1Âș 2ÂȘ
08700 Igualada (Barcelona)+34 934 894

Copyright © 2021 All rights reserved.
30+ Layouts
scroll down to view all