With thanks to the corporate partners of the 2018 EURORDIS Black Pearl Awards:
 

Tickets

Ticket sales along with corporate and individual donations go towards supporting EURORDIS’ activities in the following areas:

  • Increasing public awareness through information about rare diseases
  • Breaking the isolation of rare disease patients and their families;
  • Empowering leaders of rare disease communities through training, capacity-building activities and exchange to foster their research, therapeutic development and health policy activities.
Registration for the EURORDIS Black Pearl Awards 2019 will open in October 2018.
If you have any questions regarding the registration process, please contact:
Martina Bergna
Events Jr Manager
EURORDIS-Rare Diseases Europe
martina.bergna@eurordis.org or +33 (0)1 56 53 52 66 

 

 

How to donate to EURORDIS?

If you are unable to attend the EURORDIS Black Pearl Awards, but would like to support EURORDIS’ activities through a donation, please visit the secured donation page of our website.

Make a donation

Your donation will help to achieve our mission to work across borders and diseases to improve the lives of people living with a rare disease.

 

 

Why become a partner of this event?

The EURORDIS Black Pearl Awards are an opportunity for companies to:

  • Learn about the major achievements and advances for rare disease patients;
  • Help build awareness of achievements and positive changes which have been made by and for the rare disease community;
  • Network with other international stakeholders of the rare disease community in a neutral setting;
  • Gain visibility among stakeholders of the rare disease cause in Europe and around the world;
  • Support programmes that benefit rare disease patients on an international scale; and
  • Meet social responsibility goals to advance health and strengthen communities.

Contact: 

If your company is interested in making a gift or corporate partnership for the event, please contact
Céline Schwob, Corporate Relations Manager
EURORDIS-Rare Diseases Europe
celine.schwob@eurordis.org or +33 1 56 53 52 16