Please note that this website will be undergoing technical maintenance between 28 and 31 August. Consequently, users may experience instabilities and limited functionality. We apologise for the inconvenience.
For a better user experience please update your browser or use Chrome or Firefox browser.
Utilities
Publication detail
Home
Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 September 2019 to 30 September 2019 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)
Summary of European Union decisions on marketing authorisations in respect of medicinal products from 1 September 2019 to 30 September 2019 (Decisions taken pursuant to Article 34 of Directive 2001/83/EC or Article 38 of Directive 2001/82/EC)
Publication metadata
- Published:
- Corporate author(s): European Commission
- Subject: drug surveillance , EU Member State , market approval , marketing standard , medicinal product , veterinary medicinal product
- CELEX : 52019XC1030(03)
- OJ : JOC_2019_369_R_0002
Document viewer
Note:
The publication cannot be displayed in the document viewer. Open web version
You may access it from: Download and languages