EC regulation on conditional approval of medicinal products

 

New EU rules on conditional marketing authorisations for medicines for human use came into force at the beginning of April 2006, following a Regulation issued by the Commission on 29 March 2006 (No 507/2006).
 
Eurordis contributed to the shaping of this important regulation by submitting comments to the Commission in Jan. 2005 on the first draft regulation on conditional approval for medicinal products.
 
The regulation is of particular importance to rare diseases and orphan drugs. Conditional approval addresses situations where an urgent public health need exists, and a drug in development promises significant health benefits, but full safety or efficacy testing has not been completed. Conditional approval aims at speeding the product to market.
 
In a situation of conditional approval, the manufacturer, or "marketing authorisation holder" is committed to fulfil post-marketing obligations to obtain a definitive authorisation, based on full safety research and testing, or the product may be withdrawn from the market.

 

 
 
A voz das pessoas com doenças raras na EuropaEURORDIS A voz internacional das pessoas com doenças raras, Rare Diseases InternacionalRare Disease International Reúne doentes, famílias e especialistas para partilhar experiências num fórum multilinguístico. RareConnect O programa Rare Barometer é uma iniciativa da EURORDIS para a realização de inquéritos para transformar a experiência das pessoas com doenças raras em números e factos que podem ser partilhados com os responsáveis pela tomada de decisões.Rare Barometer An international awareness raising campaign taking place on the last day of February each year, Rare Disease Day is a EURORDIS initiativeRare Disease Day Adira ao maior encontro europeu das partes interessadas no âmbito das doenças raras na Conferência Bienal Europeia sobre Doenças Raras e Produtos Órfãos. A ECRD é uma iniciativa da EURORDISEuropean Conference on Rare Diseases