About
We provide medical writing services to the clinical trial industry. Our focus is quality.
With seven years of experience in Phase I-IV clinical development, we summarize and interpret clinical data and statistical analyses in a wide variety of therapeutic areas.
Services
Services include writing, reviewing, and editing various ICH-compliant clinical and regulatory documents, including the following:
- clinical study reports
- study protocols
- investigator brochures
- informed consent forms
- patient narratives