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