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Training and supporting materials are available from the European Medicines Agency (EMA) to help users of the Clinical Trials Information System (CTIS) comply with their legal obligations.
Veterinarians serve as the first line of defence against emerging diseases and play a crucial role in mitigating the development of antimicrobial resistance (AMR).
The European Sales and Use of Antimicrobials for Veterinary Medicine Working Group (EUSAvet) provides strategic guidance and recommendations to the European Medicines Agency (EMA) and its Committee for Veterinary Medicinal Products (CVMP). This guidance refers to the collection and analysis of data on sales volumes of veterinary antimicrobials and...
The European Union (EU) Member States and European Economic Area (EEA) countries, European Commission and European Medicines Agency (EMA) launched the Clinical Trials Information System (CTIS) on 31 January 2022.
This walk-in clinic on CTIS functionalities provides an opportunity for sponsors to receive practical information about the Clinical Trials Information System by asking questions to CTIS experts in real time.
The European Medicines Agency (EMA) is a member of the International Coalition of Medicines Regulatory Authorities (ICMRA). ICMRA is a voluntary, executive-level entity of worldwide medicines regulatory authorities set up to provide strategic coordination, advocacy and leadership.