Europos vaistų agentūra
European database of suspected adverse drug reaction reports
On this website you can view data on suspected side-effects also known as suspected adverse drug reactions for authorised medicines in the European Economic Area (EEA). For centrally...
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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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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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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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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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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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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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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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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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European Network of Centres for Pharmacoepidemiology and Pharmacovigilance (ENCePP)
The European Network of Centres for Pharmacoepidemiology and Pharmacovigilance (ENCePP®) is a network coordinated by the European Medicines Agency (EMA). The members of this network (the...
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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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European Medicines Agency's publications
Access to lists of publications (scientific articles, etc) authored by staff and experts of the European Medicines Agency.
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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.
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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 - documents open for public consultations
Access to EMA documents that are currently open for public consultation.
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European Medicines Agency - statistics on human medicines
Dataset gives access to monthly figures on centralised procedures for human medicines.
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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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Pending EC decisions on maximum residue limits (Veterinary medicines)
This search allows the user to access summaries of opinion on maximum residue limits for active substances contained in veterinary medicines, which have been assessed by the European...
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