PRTM News : EudraPharma Database- A complete & Updated Registered Drug Database of whole Europe.

EudraPharma Database

EudraPharm Database is a complete data repository of whole Europe's registered drugs for Human & Veterinary drugs can be found in complete EU including UK.

About EudraPharm
EudraPharm is intended to be a source of information on all medicinal products for human or veterinary use that have been authorised in the European Union (EU) and the European Economic Area (EEA) and information on clinical trials of medicinal products including products with or without a marketing authorization. EudraPharm has been established to fulfil Articles 57(1)(l) and 57(2) of Regulation (EC) No 726/2004.

Use of this site is subject to terms and conditions specified on the EudraPharm Notices page, which also contains Copyright and Privacy Policy information.

Languages
EudraPharm is available in the following languages:
Bulgarian, Spanish, Czech, Danish, German, Estonian, Greek, English, French, Icelandic, Italian, Latvian, Lithuanian, Hungarian, Maltese, Dutch, Norwegian, Polish, Portuguese, Romanian, Slovak, Slovenian, Finnish, Swedish

Withdrawn Products
Companies sometimes withdraw medicines from the market, and they surrender their marketing authorisation. In such cases, EudraPharm may not show any details for the presentation or the product.

Current Functionality
EudraPharm currently provides the following functionality:

Display product information for all products approved via the Centralised Procedure, as well as for some products approved via national procedures (see Data Providers).

Display Product-Information Documents for all products approved via the Centralised Procedure. The documents contain Summary of Product Characteristics, Package Leaflet and Labelling information.

Search - find product by searching for a set category of product information.

A to Z Product List - browse product details indexed alphabetically by Product Name.

Advanced Search - find product by searching for specific categories of product information.

Access to data on clinical trials - EU Clinical Trials Register.

EudraPharm is being developed in stages. Therefore, the functionality and related support will increase in future.

Future Functionality
The following functionality will be available in the future:

Ability to search all categories of product information.
Ability to register with EudraPharm so that you can set your preferences.
Ability to register for e-mail updates.
Ability to view warnings and indications.
Ability to view product information customised to the requirements of Data Providers.

EudraPharm Data Providers
The product information contained in EudraPharm is collected from the following Data Providers:
National Competent Authorities.
European Medicines Agency.

Click on the name of the Data Provider listed below to view their website. Please note that:

The EudraPharm Data Providers are not responsible for the content of external websites.
The websites do not necessarily provide product information.
The websites are only provided as a reference for further information about the Data Providers.
If you find that a link is out of date, or broken, you are invited to e-mail the EudraPharm Helpdesk to allow us to rectify the issue: <eudrapharm@ema.europa.eu>

Product information from the following Data Providers can currently be viewed in EudraPharm:

Country/Body
EudraPharm Data Provider
European Union (EU)
European Medicines Agency