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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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Sperimentazioni cliniche riguardanti la COVID-19 nello Spazio economico europeo (SEE)
Nel registro UE delle sperimentazioni cliniche (EU CTR) sono disponibili informazioni sulle sperimentazioni cliniche riguardanti la COVID-19 in corso nello Spazio economico europeo (SEE)....
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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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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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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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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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EudraGMDP database
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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Medicine data: rare disease (orphan) designations
Information on rare disease (orphan) designations based on applications that have been assessed by the European Medicines Agency's (EMA) Committee for Orphan Medicinal Products (COMP)....
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Medicine data: 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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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...
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Medicines for use outside the EU
Organizzazione mondiale della sanità
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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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