Tomić, Sinisa

Granting marketing authorisation for medicines in South East European countries: the point of view of the authority. [electronic resource] - Regulatory toxicology and pharmacology : RTP - 325-32 p. digital

Publication Type: Journal Article

1096-0295

10.1016/j.yrtph.2010.04.001 doi


Consumer Product Safety
Drug Approval--legislation & jurisprudence
Drug-Related Side Effects and Adverse Reactions
Europe, Eastern
European Union
Government Regulation
Interinstitutional Relations
Legislation, Drug
Marketing--legislation & jurisprudence
Pharmaceutical Preparations--standards