Agenzia europea per i medicinali
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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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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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Carenze di medicinali a causa della COVID-19 - elenco dei registri nazionali che riportano le carenze di farmaci
A seguito della chiusura temporanea dei siti di produzione nelle zone colpite dalla COVID-19, delle restrizioni di viaggio che incidono sulle esportazioni o di un aumento della domanda...
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Sperimentazioni cliniche riguardanti la COVID-19 nello Spazio economico europeo (SEE)
Sperimentazioni cliniche riguardanti la COVID-19 nello Spazio economico europeo (SEE) Nel registro UE delle sperimentazioni cliniche (EU CTR) sono disponibili informazioni sulle...
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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Medicine data: withdrawn applications (Human medicines)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'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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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: paediatric investigation plans (PIP)
Information on opinions and decisions adopted by the European Medicines Agency's (EMA) Paediatric Committee (PDCO) on Paediatric Investigation Plans (PIPs) including deferrals and...
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Medicine data: European public assessment reports (EPAR) for veterinary 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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Medicine data: referrals for 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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Medicine data: herbal medicines
This search allows you to find herbal substances that are designated for assessment by the European Medicines Agency's Committee on Herbal Medicinal Products (HMPC). Search results can be...
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European database of suspected adverse drug reaction reports (EudraVigilance)
The dataset provides data on suspected side-effects also known as suspected adverse drug reactions for authorised medicines in the European Economic Area (EEA). For centrally authorised...
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Parallel Distribution (PD) register
The Parallel Distribution (PD) register provides up-to-date information on parallel distribution notices checked by the European Medicines Agency to be in compliance with the conditions...
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Medicine data: periodic safety update report (PSUR) single assessments
List of major changes made to the authorisation of medicines, which have been recommended by the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) to...
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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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European Medicines Agency's event and meeting calendar
Search for all EMA events, including workshops, symposia, and Committee and Management Board meetings. Committee and Management Board meetings only display from the year 2010.
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