Committee for Orphan Medicinal Products

Committee for Orphan Medicinal Products

The Committee for Orphan Medicinal Products (COMP), headquartered in London, was created in 2000 within the European Medicines Agency (EMA) and is responsible for reviewing applications from people or companies seeking 'orphan medicinal product designation'.

Activities and role

The COMP is also responsible for advising the European Commission on the establishment and development of a policy on orphan medicinal products in the EU, and assists the Commission in drawing up detailed guidelines and liaising internationally on matters relating to orphan medicinal products.

The COMP is composed of:

  • a chair, elected by serving COMP members;
  • one member nominated by each of the 28 EU Member States;
  • three members nominated by the European Commission to represent patients' organisations;
  • three members nominated by the European Commission on the EMA's recommendation;
  • one member nominated by each of the EEA-EFTA states (Iceland, Liechtenstein and Norway);
  • one European Commission representative;
  •  observers.

See COMP members for the list of current members.

EURORDIS representation at COMP:

In addition to voting members, a number of Observers attend COMP meetings, including two EURORDIS representatives. Pauline Evers (Patients Network for Medical Research and Health, EGAN), Lesley Greene (COMP Vice-chair), Mario Ricciardi (Cystic Fibrosis Europe), Julián Isla (observer) and Virginie Hivert (observer), are the EURORDIS representatives currently present at the COMP.

Lesley Greene

Bruno Sepodes, Chair

Lesley Greene, Vice-chair

Pauline Evers

Mario Ricciardi

Virginie Hivert

Julián Isla

 

For further information:

Committee for Orphan Medicinal Products (COMP) Scientific Advice and Orphan Drugs Pre-authorisation Evaluation of Medicines for Human Use
7 Westferry Circus Canary Wharf London E14 4 HB United Kingdom
Tel: + (44-20) 74 18 84 00 Fax: + (44-20) 75 23 70 40 e-mail: info@ema.europa.eu
More information at www.ema.europe.eu.

 

Photos & graphics: © EMA

Page created: 19/08/2009
Page last updated: 23/11/2016
 
 
La voce dei malati rari in EuropaEURORDIS Rare Diseases International, la voce internazionale dei malati rariRare Disease International RareConnect è un'iniziativa di EURORDIS che mette in contatto malati, famiglie ed esperti per condividere esperienze in un forum multilingua e moderato RareConnect Il Programma Rare Barometer è un’iniziativa di EURORDIS volta a condurre indagini con l’obiettivo di trasformare le esperienze delle persone affette da malattie rare in cifre e fatti che possono essere condivisi con i decisori politici.Rare Barometer La Giornata delle Malattie Rare, una campagna di sensibilizzazione internazionale che si svolge l'ultimo giorno di febbraio di ogni anno.Rare Disease Day La Conferenza Europea biennale sulle Malattie Rare è il più grande incontro di soggetti interessati al tema delle Malattie Rare in Europa. L'ECRD è un'iniziativa di EURORDISEuropean Conference on Rare Diseases