European Medicines Agency
Treatments and vaccines for COVID-19: authorised medicines
Information on the medicines authorised in the European Union (EU) to treat or prevent COVID-19, following evaluation by the European Medicines Agency (EMA). EMA's Committee for...
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Clinical trials for COVID-19 vaccination
Information on clinical trials for COVID-19 vaccines is available in the EU Clinical Trials Register (EU CTR) Users can find information on: phase II to phase IV adult clinical...
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COVID-19 medicine shortages - list of national registers for medicine shortages
Supply disruptions or medicine shortages can occur as a result of a temporary lockdown of manufacturing sites in areas affected by COVID-19, travel restrictions impacting exports or an...
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COVID-19 clinical trials in the European Economic Area (EEA)
Information on ongoing COVID-19 clinical trials in the European Economic Area (EEA) is available in the EU Clinical Trials Register (EU CTR) Users can find information on: phase...
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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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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.
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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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All European Medicines Agency (EMA) COVID-19-related web content
The European Medicines Agency (EMA) is contributing to global efforts to save lives during the COVID-19 pandemic by expediting the development and approval of safe and effective...
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COVID-19-related ongoing observational studies in the EU
Information on ongoing COVID-19-related observational studies in the EU is available in the European Union electronic register of post-authorisation studies (EU PAS Register). Users can...
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Medicine data: 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...
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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 document library
This search allows the user to find documents published on the European Medicines Agency's website by title, reference number, document type, document owner and year of publication.
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Medicine data: 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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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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ESVAC European Surveillance of Veterinary Antimicrobial Consumption database
The European database of sales of veterinary antimicrobial agents provides public access to the data the European Surveillance of Veterinary Antimicrobial consumption (ESVAC) project...
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Medicine data: shortages
EMA assesses medicine shortages that affect or are likely to affect more than one EU Member State. Following its assessment, EMA publishes information on specific shortages and provided...
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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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The European Union Telematics Controlled Terms (EUTCT) System
EUTCT is a repository and provider of controlled terms in multiple languages for the ongoing exchange of data between information systems and applications throughout the European...
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PROTECT project - The Pharmacoepidemiological Research on Outcomes of Therapeutics by a European Consortium
The Pharmacoepidemiological Research on Outcomes of Therapeutics by a European Consortium is a collaborative European project that comprises a programme to address limitations of current...
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Medicines under evaluation (Human)
This search lists information on applications for centralised marketing authorisations for human medicines that are under evaluation by the European Medicines Agency's Committee for...
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