Agencia Europea de Medicamentos
SPOR Master Data
The service provides access to a list of multilingual master data (terminologies, classification systems, controlled vocabularies) developed in the framework of the implementation of the...
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Data from the Article 57 database on all authorised medicines
The European Medicines Agency (EMA) publishes data from the Article 57 database on all medicines authorised in the European Economic Area (EEA) such as product name, active substance,...
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European Medicines Agency's list of European experts
The European Medicines Agency (EMA) maintains a public list containing details on all European experts who can be involved in the Agency's work. The search in the database allows the...
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European Commission decisions on referrals (veterinary medicines)
The database allows the user to find information on referrals for veterinary medicines assessed by the European Medicines Agency (EMA). A referral is a procedure used to resolve issues...
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European Union Clinical Trials Register
The EU Clinical Trials Register contains information on interventional clinical trials on medicines conducted in the European Union (EU), or the European Economic Area (EEA) which started...
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European Medicines Agency - documents open for public consultations
Access to EMA documents that are currently open for public consultation.
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European Medicines Agency's publications
Access to lists of publications (scientific articles, etc) authored by staff and experts of the European Medicines Agency.
HTML (194 presentación) (46 Descargas)
EnprEMA Network Database (EnprEMA)
This database includes research networks and centres with recognised expertise in performing clinical studies in children. It is part of the European network of paediatric research at the...
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EudraGMDP is the name for the Union database referred to in article 111(6) of Directive 2001/83/EC and article 80(6) of Directive 2001/82/EC. It contains the following information:...
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The shortages catalogue contains information on medicine shortages that affect or are likely to affect more than one European Union (EU) Member State, where the European Medicines Agency...
HTML (236 presentación) (12 Descargas)
European Union Clinical Trials Register - including Article 45 Paediatric Database
Database containing data on all paediatric studies completed by 26 Jan 2007 that the marketing authorisation holders were obliged to submit to EMA by 2011.
HTML (219 presentación) (41 Descargas)
European Medicines Agency's SME Register
Public register of Small and Medium Enterprise Companies established in the European Economic Area that have submitted a SME declaration to the Agency. Register focuses on companies which...
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Paediatric investigation plans
Information on opinions and decisions adopted by the European Medicines Agency's (EMA) Paediatric Committee (PDCO) on Paediatric Investigation Plans (PIPs) including deferrals and...
HTML (247 presentación) (13 Descargas)
Withdrawn applications (Human medicines)
This dataset contains information on the decision by a pharmaceutical company to withdraw an application made to the European Medicines Agency for a human medicine. It includes...
HTML PDF (283 presentación) (16 Descargas)
Maximum residue limit assessment reports (Veterinary medicines)
This database allows the user to access the public maximum residue limit assessment reports for active substances contained in veterinary medicines, which have been assessed by the...
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Recommendations on medication errors
In order to promote the safe use of medicines, EMA systematically communicates on any additional measure decided upon at EU level to prevent medication errors. The purpose of these...
HTML (239 presentación) (6 Descargas)
EU Veterinary Medicinal Product Database
The EU Veterinary Medicinal Product Database is intended to be a source of information on all medicinal products for veterinary use that have been authorised in the European Union and the...
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Pending EC decisions (Human medicines)
In this dataset you can find medicines that have been evaluated by the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) and are currently pending a...
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European Medicines Agency's news and press release archive
Search for news and press releases published on the European Medicines Agency's website by title, committee, month and year of publication.
HTML (185 presentación) (38 Descargas)
The European public assessment reports (EPAR) for human medicines
The EMA publishes an EPAR for every medicine granted a central marketing authorisation by the European Commission following an assessment by the EMA's Committee for Medicinal Products for...
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