Would you like to conduct a clinical trial with main focus on the patient rather than administration?
I am able to offer support!
- Creation of all documents
- Trial Master File (TMF)
- Investigator Site File (ISF)
- Case Report Form (CRF)
- Investigator Brochure (IB)
- Study Protocol
- Clinical study report
- Patient consent form
- Data protection declaration
- Ethical approval
- Training material
- Selection of centers
- Clinical monitoring
- Data Management
- Preparation and writing of publications for international and German journals
- Preparation of presentations, abstracts and posters