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Research Clinical Research Support

About

Within Radboudumc, there are various possibilities for support in the design, conduct and completion of (clinical) human-related scientific research. These are facilitated by three teams, which are organized within our research institute.

How can we help you?

Team Clinical Research Policies

We develop policy and we advise and support researchers and research staff to comply with all laws and regulations in the design, conduct and completion of human-related scientific research in which Radboudumc is a provider or participating center.

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Team Clinical Research Monitoring

We provide qualified monitors to be used for research commissioned by Radboudumc. Our monitors can be involved for any type of research. In moderate- and high-risk studies, you are required to engage our team for monitoring.

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RTC Clinical research unit

We provide qualified personnel, research rooms and equipment needed to conduct clinical research according to applicable laws, regulations and policies. We provide customized support for start-up and implementation of any type of human-related research.

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Local feasibility, VGO and WMO-subject insurance

For WMO-compliant research in which Radboudumc acts as sponsor or participating center, approval must be granted by the Radboudumc Executive Board prior to the start of the research. We coordinate the approval procedure and assess the content of the file as a means of quality assurance.

Research monitor accounts for external parties

We handle the issuance of research monitor accounts for monitor visits by an external party. This allows external monitors, subject to permission, to view and verify data of Radboudumc research participants.

Services for our employees

If you are logged in to intranet (purple dot in the right-hand column showing your initials), the overview above also shows services available only to our researchers and research staff (indicated with a lock).