We ensures that all documents meet the required submission standards
As part of the Biometrics department, the medical writer will work in close cooperation with statisticians, data managers and experts in regulatory affairs. This ensures that all documents meet the required submission standards.
Our services include the writing of documents for regulatory/pharmaceutical purposes and for all other medical communication.
Services within Medical writing:
- Clinical study reports (phases I-IV)
- Clinical study protocols
- Investigators’ brochures
- Patient narratives/safety reports
- Manuscripts for publication in peer-reviewed scientific journals
- Literature reviews