Salerno Scientific, LLC 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.

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