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- CTIS Reference Faomhadh an téarma seo mar chuid de Thionscadal Lex
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- an Córas Faisnéise maidir le Trialacha Cliniciúla Reference Rialachán Cur Chun Feidhme (AE) 2022/20 lena leagtar síos rialacha maidir le cur i bhfeidhm Rialachán (AE) Uimh. 536/2014 ó Pharlaimint na hEorpa agus ón gComhairle a mhéid a bhaineann le bunú na rialacha agus na nósanna imeachta um chomhar idir na Ballstáit sa mheasúnú sábháilteachta ar thrialacha cliniciúla, CELEX:32022R0020/GA Faomhadh an téarma seo mar chuid de Thionscadal Lex
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- CTIS | Informationssystem für klinische Prüfungen
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- Definition System, das von der Europäischen Arzneimittel-Agentur in Zusammenarbeit mit den Mitgliedstaaten und der Europäischen Kommission eingerichtet und gepflegt wird und das zentrale EU-Portal sowie die EU-Datenbank für klinische Prüfungen enthält, die gemäß der Verordnung (EU) Nr. 536/2014 erforderlich sind Reference COM-DE nach:European Medicines Agency > Human regulatory > Research and development > Clinical trials > Clinical Trials Regulation (22.12.2021)
- CTIS | Clinical Trials Information System
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- Definition system set up and maintained by the European Medicines Agency, in collaboration with the Member States and the European Commission, which contains the centralised EU portal and database for clinical trials provided for in Regulation (EU) No 536/2014 Reference COM-Terminology Coordination, based on: EMA (European Medicines Agency). 'Clinical Trials Regulation' (8.12.2021)
- Comment EU portal (Article 80) and database (Article 81) for clinical trials provided for in Regulation (EU) No 536/2014