Dossier for marketing authorization in the European union
Extensive and complete documentation must be presented for marketing authorization of a medicinal product in the EU. Presented documentation should prove quality, safety and efficacy of the medicinal product. It is ensured that the applicant supplies the authorities with complete information. The l...
Main Author: | Maida Todić |
---|---|
Format: | Article |
Language: | English |
Published: |
Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina
2003-02-01
|
Series: | Bosnian Journal of Basic Medical Sciences |
Subjects: | |
Online Access: | http://www.bjbms.org/ojs/index.php/bjbms/article/view/3572 |
Similar Items
-
Improving the Tenure Committee's Review Efficiency with Embedded Dossier Functionality
by: Brian Henriksen, et al.
Published: (2015-01-01) -
Dossier Archai: Voces Socráticas - Presentación
by: Rodrigo Illarraga, et al.
Published: (2021-06-01) -
Presentación del dossier
by: Gabriela Milone
Published: (2015-12-01) -
Dossier. Ciencia y cultura visual
by: Piroska Csúri, et al.
Published: (2014-11-01) -
Regulatory requirements for the registration of generic medicines and format of drug dossiers: procedures in Sri Lanka in comparison with selected regulatory authorities
by: D. Thambavita, et al.
Published: (2018-06-01)