Responsibilities and Services
The requirements for clinical studies, which are legally regulated, are complex and extensive and require dedicated time for administrative and coordinative handling.
The CTC-A serves as a central point of contact for involved project partners in the self-initiated research of the interdisciplinary and multi-professional project teams. It is also the contact for external offices such as ethics committees, agencies, and finaciers.
All relevant aspects of clinical examination are identified, recorded, and prepared for a successful approval processes among ethics committies and agencies within a timely fashion in accordance with the AMG, MPG, or BOÄ. The CTC-A ensures that there is appropriate, overarching communication between all the involved institutions and partners.
Support for researchers in individual and needs-based. All services with costs are available individually.
|Basic Services – free up to 54 hours||Services – for a fee*|
|Full cost calculation (Industry and IIT)||Creation of a study protocol|
|Contract review||Requests for insurance|
|Entry into the register of clinical trials
|Proposals to ethics committees and agencies|
|Support with funding proposals||Project management|
|General clinical trial advising||Integrative management & correspondence|
|Creation of documents|
|Creation of annual reports|
|Management of unwanted events|
|Flying Study Nurse|