Regulatory writing *
- Clinical study protocols
- Informed consent forms
- Clinical study reports
- Common technical document (Section 2.5 [clinical overview] and Section 2.7 [clinical summaries])
- Investigator brochures
Publication writing *
- Abstracts
- Posters for conference presentation
- Slidekits for conference presentation
- Manuscripts (primary articles or reviews)
Medical affairs and medico-marketing writing *
- Expert medical documentation for medical affairs communities or regulatory agencies, produced in conjunction with the medical experts
- Product monographs
- Product support products (e.g. information leaflets for patients, doctors, or the general public)
- Summaries of publications to support marketing needs
* = non-exhaustive list. For any enquiry not listed here, please contact me.