Orphan medicinal products - the role of the EMEA

Pharmaceuticals Policy and Law

Volumn 3, Issue , 2001, Pages 31-35

  Courtoisa, Patrick Le ^a   Carr, Melanie ^a  

^a EUROPEAN MEDICINES AGENCY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 85013590966     PISSN: 13892827     EISSN: 2210495X     Source Type: Journal    
DOI: None     Document Type: Article

References (4)

1. Regulation (EC), No 141/2000 of the European Parliament and the Council of 16 December 1999, (OJ L18/1, 22.1.2000).
2. Commission Regulation (EC), No 847/2000 of 27 April 2000, (OJ L103/5, 28.4.2000).
3. Council Regulation (EC), No 2309/93 of 22 July 1993, (OJ L214, 24.8.1993).
4. Draft Guideline on the Format and Content of Applications for Designation as Orphan Medicinal Products, European Commission Enterprise Directorate-General, ENTR/6283/00, 18 April 2000.