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Legislative status and clarifications regarding the submission dossier as well as the duration of the approval of clinical trials in Romania in 2022, considering the transition from the European Directive to the new Clinical Trials regulation EU No. 536/2014

We are excited to announce to you that Avantyo Institute of Clinical Research continues this year the series of round table meetings with the competent authorities organized for discussion about clinical trials development in Romania.

On May 10th, at 12 o’clock P.M.we will gather to discuss about “Legislative status and clarifications regarding the submission dossier as well as the duration of the approval of clinical trials in Romania in 2022, considering the transition from the European Directive to the new Clinical Trials regulation EU No. 536/2014”

As is well known, Avantyo Institute of Clinical Research is a mediator of discussion with the only purpose to stregthen relationship between Romanian competent authorities and pharma & CROs industry representatives as long with investigators, patient associations and other clinical trials specialists.

Find out more: here.

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