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Begriffe, Krankheiten, Einrichtungen u.v.m., verknüpft mit dem zuständigen Bereich.
Begriffe, Krankheiten, Einrichtungen u.v.m., verknüpft mit dem zuständigen Bereich.
Suche über die Einrichtungen
Im Menüpunkt "Übersicht" sind Einrichtungen unter verschiedenen Gesichtspunkten gruppiert: Kliniken, Abteilungen, Institute, Zentrale Einrichtungen und ähnliches.
Im Menüpunkt "Übersicht" sind Einrichtungen unter verschiedenen Gesichtspunkten gruppiert: Kliniken, Abteilungen, Institute, Zentrale Einrichtungen und ähnliches.
Members of staff
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Dr. Annette Uhlmann Project Coordinator Clinical Trials Tel. 0761/270-74030 annette.uhlmann@uniklinik-freiburg.de |
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Dr. Sabine Schneider-Fuchs Project Coordinator Clinical Trials Tel. 0761/270-74040 sabine.schneider-fuchs@uniklinik-freiburg.de |
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Ralf Tostmann Project Coordinator Clinical Trials Tel. 0761/270-77110 ralf.tostmann@uniklinik-freiburg.de |
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Christine Winterhalter
Medical Documentation Tel. 0761/270-77760 christine.winterhalter@uniklinik-freiburg.de |
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Arthur Allignol Coordinator Biometry Tel. 0761/270-77850 arthur.allignol@uniklinik-freiburg.de |
Service
The Clinical Trials Office CCI runs in close cooperation with the Clinical Trials Unit of the University Hospital Freiburg. We provide assistance for clinical trials, non-interventional and epidemiological studies, from the planning phase until the end of the study. To this end an interdisciplinary team of medical doctors, project coordinators and study assistants work very closely together.
Our aim is to provide the best possible support for a clinical study from both the medical and organisational perspectives. We provide information on participation in clinical trails in general as well as on clinical trials conducted in our department.
Below is a range of services provided by the Clinical Trials Office CCI:
- Examination of concepts of planned studies both for national and international clinical studies (design, funding)
- Evaluation of the feasibility of a particular clinical study in regard to the practicalities involved (e.g. patient collective, legal requirements)
- Contract management
- Organisation of resources for clinical monitoring and data management
- Coordination of biometrics and medical writing for study evaluation





