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Check the national registers of authorised medicines for finding medicines authorised via national procedures. The European Medicines Agency (EMA) facilitates development and access to medicines for countries within the European Union (EU).
- National Registers
The national medicine registers in the different Member...
- Medicines Under Evaluation
For information on treatments and vaccines for COVID-19,...
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These pages also contain information on medicines for which...
- National Registers
Approved Marketing Authorisations (MA) containing Acetavance in Europe. Original Data : EMA Website
Search our Certification database for information on Certificates of Suitability (CEPs) granted by the EDQM. The Standard Terms database contains terms and definitions to describe pharmaceutical dose forms, routes and methods of administration, containers, closures and administration devices and patient-friendly terms.
The national medicine registers in the different Member States of the European Union (EU) and European Economic Area (EEA) contain information on medicines authorised in those countries, including links for the summary of product characteristics (SmPC) and the package leaflet.
Search for chemicals This is unique source of information on the chemicals manufactured and imported in Europe. It covers their hazardous properties, classification and labelling, and information on how to use them safely.
Bureau Veritas Approval Explorer allows you to identify, locate and contact an approved service supplier or approved product manufacturer. Search for Service suppliers involved
Once granted by the European Commission, the centralised marketing authorisation is valid in all European Union (EU) Member States, Iceland, Norway and Liechtenstein. Follow the journey of a medicine for human use assessed by EMA in this interactive timeline.
