Salerno Scientific LLC offers medical writing and consulting about pharmaceuticals and biotechnology. You can expect an experienced hand with what you need, including:

  • Clinical study reports
  • Pediatric study plans (FDA)
  • Paediatric investigation plans (European Medicines Agency)
  • White papers
  • Orphan drug applications
  • SOP manual, style guides
  • Modules 2.7.3 Summary of Clinical Efficacy, 2.7.4 Summary of Clinical Safety
  • 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.