We accompany your project from the initial idea to completion and beyond.
Our goal is to enable the creation of your documents quickly, cost-effectively and compliant with regulations.
We offer you not only advice but also the preparation and correction of study-specific documents. Of course, all information will be kept strictly confidential.
Below is a selection of our services for medical writing:
- Clinical investigation plan / synopses
- Patient consent
- Patient information
- CRFs (case report forms)
- Investigator site file (ISF)
- Patient diaries
- Processing of Authorities and Ethics Committees checklists
- Registration of clinical studies
- Interim / Final report