Our clinical writing team consists of physicians with long-standing experience in a wide range of scientific fields.

The substantial transformation of premises and results into report and documentation, considering the standards of regulation in corresponding scientific areas, realizes the functional output of your clinical trial and researches. 

In conclusion, our clinical writing services include the concept, development, design, and review of 

• trial protocols, synopses, and amendments 
• informed consent forms 
• patient information forms and leaflets
• case report forms, patient diaries, and questionnaires 
• integrated clinical study reports (incl. "Mock", interim, and abbreviated reports) 
• relevant parts of the Common Technical Document (CTD) 
• manuscripts, abstracts, and posters 

English trial documents will be translated according to local regulations, as required.