Task 8.5. Information provision during the conduct of the clinical studies related to study progress, data quality and data safety of the clinical studies

During the conduct of the clinical studies CRISP will have a central role in providing information related to study progress, data quality and data safety of the clinical studies. Information will be provided in cooperation with the various WPs. Online reports will be implemented to facilitate the monitoring of real time study progress and dedicated off-line reports will be developed and updated on regular and ad-hoc basis for various requirements (e.g. related to data quality, data safety and support of data monitoring activities).

Contact us

Coordinator:

Herman Goossens

Herman.Goossens@uza.be

Deputy Coordinator:

Menno de Jong

m.d.dejong@amc.uva.nl

prepare@uantwerpen.be

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