3rd Workshop, Barcelona: “Rare Disease Clinical Trials: Ensuring Fruitful Collaborations between Sponsors & Patient Organisations”

3rd Workshop of the Eurordis Round Table of Companies:

“Rare Disease Clinical Trials: Ensuring Fruitful Collaborations between Sponsors & Patient Organisations”

 

November 21st, 2005

Barcelona, Spain

participants discussing among themselvesAn advanced draft of the EURORDIS Charter for Clinical Trials in Rare Diseases was presented to the ERTC members who attended this workshop and a consultation phase was launched for all the ERTC members, which lasted a few months. They were asked to help EURORDIS to prepare the most useful and appropriate document to help sponsors to conduct their studies with direct collaboration and involvement of rare disease patients' organisations.

Participants: 56

Key feature: first presentation of the draft EURORDIS Charter for rare disease clinical trials

Programme

Concept Paper

Proceedings

For ERTC Members only, this document is password protected. If you want to become a member, find out more here or contact Anne-Mary Bodin, Operations Assistant.

 

 
 
La voz de los pacientes de enfermedades raras en EuropaEURORDIS La voz internacional de las personas que tienen enfermedades rarasRare Disease International Reuniendo a pacientes, familiares y expertos para compartir experiencias en un foro moderado en distintos idiomas. RareConnect El Programa Rare Barometer es una iniciativa de EURORDIS que realiza encuestas para transformar las experiencias de los pacientes con enfermedades raras en cifras que puedan compartirse con los responsables políticos.Rare Barometer Una campaña internacional de sensibilización que se celebra todos los años el último día de febrero, El Día de las Enfermedades Raras es una iniciativa de EURORDISRare Disease Day Únete al mayor grupo de partes interesadas en toda Europa, en la Conferencia Europea sobre Enfermedades Raras y Medicamentos Huérfanos que se celebra cada dos años. ECRD es una iniciativa de EURORDISEuropean Conference on Rare Diseases