Orphan medicinal products
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Patients suffering from rare diseases deserve the same quality of treatment as other patients within the European Union.
Given the small numbers of patients affected by rare diseases, the pharmaceutical industry has been reluctant in the past to invest in the research and development of medicinal products to treat them.
The EU introduced new legislation in 2000 with the aim of providing incentives for the development of medicines for rare diseases (so-called orphan medicinal products).
Orphan medicinal products
Latest orphan medicinal products
Latest orphan designations
EU action on orphan medicinal products
The EU Regulation on orphan medicinal products establishes a centralised procedure for the designation of orphan medicinal products and puts in place incentives for their research, development and marketing.
Pharmaceutical companies can benefit from incentives such as fee waivers, scientific assistance for marketing authorisation and the possibility of an EU marketing authorisation with a 10-year market exclusivity period.
The Committee for Orphan Medicinal Products (COMP) in the European Medicines Agency, is responsible for the scientific examination of applications for approval of orphan medicinal products.
Review of EU orphan legislation
Impact of EU orphan regulation
Since 2000, the European Commission has published a number of reports on orphan medicinal products. They reveal an annual increase in the number of orphan medicinal products being authorised, since the Regulation entered into force.
- Inventory of EU and national incentives to support research and development:
- 2006 report on the application of EU Orphan Regulation
Guidelines on EU orphan medicines legislation
- Commission Regulation (EC) No 847/2000 laying down implementing rules and definitions for the application of the Regulation
- Commission Notice on the application of Articles 3, 5 and 7 of the Orphan Regulation (replacing the 2003 Commission Communication)
- Article 8(2) of Regulation No 141/2000
- Article 8(1) and 8(3) of Regulation No 141/2000
- EU guideline on the format and content of applications for designation as orphan medicinal products and on the transfer of designations from one sponsor to another (March 2014)
- Annex to Guideline PDF format - Word format.
Related information
Nové
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Publikované12 Január 2021V rubrike: Lieky určené pre ľudí
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Publikované05 Január 2021V rubrike: Lieky určené pre ľudí
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Publikované14 December 2020V rubrike: Lieky určené pre ľudí
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