Europe: High Cost Orphan Drug Treatments for Rare Diseases become Controversial

Report Buyer, the online destination for business intelligence for major industry sectors, has added a new report.
By: Joe Walsh
 
June 14, 2011 - PRLog -- According to a new report titled “Orphan Drugs in Europe: Pricing, Reimbursement, Funding and Market Access Issues” available at http://www.reportbuyer.com/go/JPR00002 the orphan drug market faces hurdles at a national, regional and local level. This 143 page report analyses what these are and the strategies employed by successful orphan drug companies.

The price of treating uncommon diseases in a period when austerity measures are affecting total healthcare funding throughout Europe is a very controversial topic. There is a certified and urgent clinical need, a high patient demand and the treatments themselves can often offer the only hope. The report aims to determine if this is argument enough to declare premium prices and special status in a time of budget limitations, and strong demand for proof of clinical and cost effectiveness.
   
The orphan drug regulation no.141/2000, resulting in 724 selected products and 62 marketing approvals in the first 10 years, has without doubt been one of the most successful legislative processes taken by the EU. Boosting development and accelerating regulatory approval are very important, but alone do not guarantee orphan drugs are actually available for use. Rare disease patients need suitable access to therapies that are wholly funded by social health insurance and national health services.

The report “Orphan Drugs in Europe: Pricing, Reimbursement, Funding and Market Access Issues” is available from Report Buyer at:
http://www.reportbuyer.com/pharma_healthcare/prescription...

Reportbuyer Product Code: JPR00002
   
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Source:Joe Walsh
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Tags:Orphan, Drug, Europe
Industry:Drug
Location:London City - London, Greater - England
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