Simone Boselli

  • Public Affairs Director

Simone Boselli

Simone Boselli joined EURORDIS in April 2017 as a Public Affairs Director.  

A member of the European and International Advocacy team, Simone contributes to European policy development and specifically represents EURORDIS in policy discussions on access to therapies, with a focus on reducing delays and inequalities, on the underlying challenges in the field of the value assessment, pricing and reimbursement of orphan medicines, and on current initiatives towards improved access (e.g. MoCA). He has contributed to the finalisation of the paper on 'Breaking the Access Deadlock to Leave No One Behind' and is engaged in finding new policy solutions for improving access to innovative therapies for people with rare diseases.

With a view to advance rare diseases as a public health priority at a global level, Simone also supports advocacy activities at Rare Diseases International and the further development of NGO Committee for Rare Diseases.

Simone brings to EURORDIS over ten years of experience in the European public affairs arena, having previously worked for two leading consultancies in Brussels and specialised in health advocacy and government affairs in particular. He has in-depth expertise in healthcare having devised and implemented advocacy campaigns at EU and national level on a range of global health issues from sustainable health systems, chronic diseases, healthy ageing to mental health, neurodegenerative diseases, malaria, TB and hepatitis C.

Simone graduated in Sciences of Communications at the University of Bologna and holds a post-graduate certificate in European Public Relations and Project Management from the Italian Institute of Commerce in Brussels.

Simone speaks Italian, English and French, and has a working knowledge of Spanish. 

Telephone: +32 2 274 06 13
Email: simone.boselli@eurordis.org

 
 
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