Medical Writing
We have a strong expertise in the preparation of regulatory and medico-marketing documents.
Regulatory Documents
- Clinical trial reports, Phase I-IV (ICH 3 or company specific SOPs)
- CTD: Clinical and non-clinical summaries, clinical overviews
- Observational and epidemiological study reports
- Patient survey reports
- Periodic Safety Update Reports (PSUR)
Medical Communication
- Publication strategy
- Preparation and submission of manuscripts for publication
- Conference reports
- Medico-marketing brochures
- Specific marketing documentation