Services and databases
The European Medicines Agency (EMA) hosts a number of websites and systems to support its work. You can browse a selection of these below, A-Z.
Corporate
Clinical trials in the European Union
A centralised system for managing clinical trials in the EU and EEA, with publicly available information on clinical trials granted or refused permission via the system
EMA Account Management
Used for creating and managing EMA user accounts, which users need for accessing certain services and systems managed by EMA
eSubmission
Used by pharmaceutical companies to submit regulatory information concerning marketing authorisations applications to the national competent authorities and EMA
European database of suspected adverse drug reaction reports
Contains suspected side effects reported by patients and healthcare professionals in the EU, with information on how to interpret them
IRIS
Used by pharmecutical companies for handling product-related scientific and regulatory procedures with EMA, with certain information accessible to all visitors
Product Lifecycle Management Portal (PLM)
Used by pharmaceutical companies and regulators for managing medicine-related product data, with read-only access for visitors
Substance, product, organisation and referential (SPOR) data management services
Used by pharmaceutical companies and regulators for managing medicine-related master data, with read-only access to all visitors
Veterinary medicines information website
Information on authorised veterinary medicines across all EU / EEA countries, including their availability in specific countries