Salerno Scientific offers medical writing and consulting about pharmaceuticals and medical devices. You can expect an experienced hand with what you need, including:
- Clinical study reports
- Pediatric study plan (FDA)
- Paediatric investigation plan (European Medicines Agency)
- White papers
- Orphan drug applications
- SOP manual, style guides
- 510(k) submissions
- Informed consent documents
- Briefing documents
- Seminars on ICH, GCP, the CTD, and Statistics in Medicine.
With first-hand knowledge of the industry, you receive service by a professional with a deep understanding of clinical trials. You can expect successfully managed projects completed with high-quality results. You have a commitment from start to finish, to get your job done right, the first time.