Clinical studies Our mission and vision
Our mission is to optimally facilitate clinical research. In our Radboudumc Technology Center (RTC) Clinical studies knowledge, expertise and capacity for conducting clinical studies and scientific research merge.
read moreClinical studies Our mission and vision
Our mission is to optimally facilitate clinical research. In our Technology Center knowledge, expertise and capacity for conducting clinical studies and scientific research merge. This allows us to guarantee the same high level of quality at every research location, in a safe, fast, cost-effective and innovative way. With our Technology Center, Radboudumc has the ambition to excel in clinical research. This contributes significantly to meaningful health care.
Services & expertise
We offer support in all phases of clinical research, varying from project management to monitoring.
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It is important that you, as a researcher or research staff, comply with the increasingly stringent laws and regulations concerning research in human subjects.BROK course
As a researcher, having a valid BROK certificate is mandatory to conduct research in human subjects. The RTC Clinical studies has a local BROK coordinator to whom you can address your questions, and also provides the center-specific meeting as part of the basic course BROK and the re-registration training.GCP course
BROK is not mandatory for research staff. A WMO / GCP certificate will suffice. The RTC Clinical studies can provide tailor-made training on request. The RTC Clinical studies can also be approached for refresher training.Basic course Monitoring
The basic training course Monitoring of research in human subjects with a negligible risk is offered by the RTC Clinical studies. At the end of the course, participants are able to independently carry out monitoring visits for investigator initiated and WMO-related research with a negligible risk.We also provide training for biomedical / medical students on various (research) modules in both the Bachelor and Master phase.
Further information? Contact the RTC Clinical studies via email or tel: +31 (0) 24 366 83 33.
Local feasibility application and coordination
The RTC Clinical studies coordinates the procedure for obtaining approval from the Board of Directors of Radboudumc for the execution of (mono and multicenter) trials falling under the Medical Research Involving Human Subjects Act (WMO).
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