Our dedicated Medical Writing team can provide the full range of medical documents required for your clinical program. This team is composed of highly competent professionals with fluency in English, French and Dutch, and includes native English speakers.
We can write, review, perform quality control, edit, and translate a broad portfolio of documents produced in accordance with the International Conference on Harmonisation (ICH) guidelines, including:
- Investigational Medicinal Product Dossiers
- Investigator's brochures
- Clinical study protocols
- Informed consent forms
- Clinical study reports
- Standard Operating Procedures