CTIS

EMA’s Clinical Trials Information System (CTIS) goes live

NewsPar Ngangta Mbaidoum 1 février 2022

The European Medicines Agency’s (EMA) Clinical Trials Information System (CTIS) has gone live as of January 31st. CTIS is the backbone of the Clinical Trials Regulation that will harmonise the assessment and supervision of clinical trials in the European Union. The Clinical Trials Regulation and CTIS will strengthen clinical trials in the EU, ensuring better…

EMA Webinar for SMEs and Academia on the Clinical Trial Regulation and the Clinical Trials Information System

NewsPar Ngangta Mbaidoum 14 octobre 2021

The European Medicines Agency (EMA) is organising a webinar for small and medium enterprises (SMEs) and academia on the Clinical Trial Regulation (Regulation (EU) No 536/2014) and the Clinical Trials Information System (CTIS). The webinar will take place on November 29, 2021 from 09.00 – 13.15 CET. The webinar is being organised as a training event and will present: an…

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CTIS

EMA’s Clinical Trials Information System (CTIS) goes live

EMA Webinar for SMEs and Academia on the Clinical Trial Regulation and the Clinical Trials Information System

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