NAMSA provides professional report writing and manuscript submission services to medical device manufacturers. We employ postgraduate-level clinical and scientific experts who have contributed in part or in whole to clinical reports for regulatory submissions and academic journals. Together with colleagues in our biostatistical, clinical, and regulatory groups, our writers organize, interpret, and present data in the most accurate and persuasive manner possible.
Common Report and Manuscript Writing Assignments
- Interim and final clinical reports
- Sections of interim and final clinical reports
- Ghost-writing for academic journal manuscripts
- Co-authorship to journal submissions
- Literature summaries
- Expert opinion letters
- Review and editing
- Regulatory submissions
- Advisory panel presentations