Medical writing is an integral part of all phase I-IV clinical research. The progression of compound in the development process hinges on the data obtained from clinical trials and its accurate presentation and interpretation.
Therefore, Symbiorph Clinical Trialogy understands that well written clinical trial documents are an extremely important link in the whole process of clinical research. We have teams of experienced medical writer's which helps our client to realize their medical writing needs.
Our medical writing services include:
- Clinical study protocol
- Investigator brochures
- Case Report Form
- Patient informed consent forms
- Translation service
- Serious adverse event report
- Preparing Periodic Safety Update Reports (PSURs) documents
- ICH E3-compliant clinical report format
- Preparing clinical sections of the Common Technical Document (CTD)
- Literature reviews
- Posters, abstracts, and manuscripts
