9th Workshop, Paris: "Significant Benefit of Orphan Drugs:Impact on Clinical Development and Assessment"

9th Workshop of the Eurordis Round Table of Companies:

"Significant Benefit of Orphan Drugs:Impact on Clinical Development and Assessment"

 

December 12th, 2008

Paris, France

L'Aero-club    de France interiorFurther to the revision of the EMEA Recommendation on significant benefit and the increasing discussions on added-value of orphan drugs at European level, this meeting provided a good forum to discuss how significant benefit can be linked to the post-marketing assessment of Orphan Medicinal Products in the Member States.
Among the meeting outcomes, we can highlight the consensus on the need to communicate to the public on significant benefit. Greater transparency on the benefit provided by each new orphan drug authorised in Europe will certainly have an impact on the use of orphan drugs by physicians and patients, and, in general, on the recognition of the value of these products by national authorities and society at large.

Participants: 48

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