Leit í EES-gagnagrunni
Commission Directive 91/356/EEC of 13 June 1991 laying down the principles and guidelines of good manufacturing practice for medicinal products for human use
COM(1998) 450
Regulation (EC) No 141/2000 of the European Parliament and of the Council of 16 December 1999 on orphan medicinal products
Reglugerð Evrópuþingsins og ráðsins (EB) nr. 141/2000 frá 16. desember 1999 um lyf við fágætum sjúkdómum