EMA certifies Sermes CRO as a key entity in the CTIS Training plan

Sermes CRO has been elected by the EMA as “Train of trainers” for the new Clinical Trial portal, CTIS (Information System).

Sermes CRO: Updated info about The EMA´s new EU portal of clinical trials (CTIs)

The European Medicines Agency (EMA) aims to have its Clinical Trial Information System (CTIS) ready by December 2021, committing itself to this objective in updating its plans for 2021.

The EMA & The FDA co-presede the first regulatory workshop on Covid-19 for vaccine development

Yesterday 18th of March, 2020, the first global regulatory workshop on COVID-19, was convened under the umbrella of the International Coalition of Medicines Regulatory Authorities (ICMRA).