EudraCT (European Union Drug Regulating Authorities Clinical Trials) is the European clinical trials database of all clinical trials of investigational medicinal products with at least one site in the European Union commencing 1 May 2004 or later. The EudraCT database has been established in accordance with Directive 2001/20/EC. The EudraCT Number is unique and is needed on other documents relating to the trials (e.g. SUSAR reports). No new EudraCT numbers are issued since February 2023. They have been replaced by EU CT numbers.
The public side of EudraCT is for organisations to register any of their clinical trials as defined by Directive 2001/20/EC. The process of applying and registering a clinical trial should be completed before submitting an application to any of the Member State/s in which they anticipate running the trial. The public side of EudraCT does not save any of the trial detail entered by the user, and instead provides a saved data file in the form of an XML which the user must store on their own local hard drive.
Application for a EudraCT number is made via the EudraCT website. To generate the EudraCT number some basic information about the requestor's organisation and the trial is required:
Once the requestor submits the form, the EudraCT Number will be assigned and an e-mail called "EudraCT Receipt" sent. The EudraCT number has the format YYYY-NNNNNN-CC, where:
The Clinical Trial Application (CTA) form is also created via the EudraCT system.
The EudraCT database is currently on Version 9.
Version 9 of EudraCT was released in November 2013.
New features for Version 9 include:
Protocol-related information
Sponsors can:
PIP addressees can:
Result-related information
Results users can:
Country | Organisation | Website | |
---|---|---|---|
Austria | Bundesamt für Sicherheit im Gesundheitswesen (BASG) | http://www.basg.at/ | |
Belgium | Federaal Agentschap voor Geneesmiddelen en Gezondheidsproducten (AFMPS) | http://www.fagg-afmps.be/ | |
Bulgaria | Bulgarian Drug Agency (BDA) | http://www.bda.bg/ | |
Croatia | Agencija za lijekove i medicinske proizvode | http://www.almp.hr/ | |
Cyprus | Ministry of Health - Pharmaceutical Services | http://www.moh.gov.cy/ | |
Czech Republic | Státní ústav pro kontrolu léčiv (SÚKL) | http://www.sukl.cz/ | |
Denmark | Danish Medicines Agency (DKMA) | http://laegemiddelstyrelsen.dk/ | |
Estonia | State Agency of Medicines (SAM) | http://www.ravimiamet.ee/ | |
Finland | Fimea | http://www.fimea.fi/ | |
France | Agence Nationale de Sécurité du Médicament (ANSM) | http://ansm.sante.fr/ | |
Germany | Bundesinstitut für Arzneimittel und Medizinprodukte (BfArM) | http://www.bfarm.de/ | |
Germany | Paul-Ehrlich-Institut (PEI) | http://www.pei.de/ | |
Greece | National Organisation for Medicines (EOF) | http://www.eof.gr/ | |
Hungary | National Institute of Pharmacy and Nutrition (OGYÉI) | https://www.ogyei.gov.hu/ | |
Iceland | Lyfjastofnun (IMCA) | https://web.archive.org/web/20111003224256/http://www.imca.is/ | |
Ireland | Health Products Regulatory Authority (HPRA) | http://www.hpra.ie/ | |
Italy | Agenzia Italiana del Farmaco (AIFA) | http://www.agenziafarmaco.gov.it/ | |
Latvia | Zalu Valsts Agentura (ZVA) | http://www.zva.gov.lv/ | |
Liechtenstein | Amt für Gesundheit (AG) | https://web.archive.org/web/20111024152641/http://www.ag.llv.li/ | |
Lithuania | Valstybine Vaistu Kontroles Tarnyba (VVKT) | http://www.vvkt.lt/ | |
Luxembourg | Division de la Pharmacie et des Medicaments | http://www.etat.lu/MS | |
Malta | Medicines Authority | http://medicinesauthority.gov.mt/ | |
Netherlands | Centrale Commissie Mensgebonden Onderzoek (CCMO) | http://www.ccmo.nl/ | |
Norway | Statens Legemiddelverk (NOMA) | http://www.noma.no/ | |
Poland | Urząd Rejestracji Produktów Leczniczych (URPL) | http://www.urpl.gov.pl/ | |
Portugal | Autoridade National do Medicamento e Produtos de Saude I.P. (Infarmed) | http://www.infarmed.pt/ | |
Romania | Agentia Nationala a Medicamentului si Dispozitivelor Medicale (ANMDM) | https://www.anm.ro/ | |
Slovakia | Slovakia Medicines Agency | http://www.sukl.sk/ | |
Slovenia | Javna Agencija Republike Slovenije za Zdravila in Medicinske Prioimocke (JAZMP) | http://www.jazmp.si/ | |
Spain | Agencia Española de Medicamentos y Productos Sanitarios (AEMPS) | http://www.aemps.gob.es/ | |
Sweden | Lakemedelsverket | http://www.lakemedelsverket.se/ | |
UK | Medicines and Healthcare Products Regulatory Agency (MHRA) | http://www.mhra.gov.uk/ |