July 13, 2017

The subject of non-commercial trials are drugs already marketed and it is not intended to investigate and introduce new innovative products but to analyze the efficacy of different doses of medication in different indications (eg. pediatric). This approach allows to br...

July 13, 2017

Clinical Trial Application | All Member States will have to follow the same rules and time requirements when evaluating CTA. CTA will be submitted by EU portal and sponsor shall propose one of the Member States concerned (MSC) as reporting Member State (RMS).

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