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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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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: 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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Medicine data: referrals for human medicines
This search allows the user to find information on referrals for human medicines assessed by the European Medicines Agency (EMA). It includes ongoing and completed referral procedures....
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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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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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EMA Medicine evaluation figures (veterinary medicines)
The European Medicines Agency (EMA) publishes information on the volume and outcome of marketing authorisation and post-authorisation applications for veterinary medicines that it...
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EMA Medicine evaluation figures (human medicines)
The European Medicines Agency (EMA) publishes information on the volume and outcome of marketing authorisation and post-authorisation applications for human medicines that it evaluates.
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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: 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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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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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: 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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