Medical Writing

Medical writers consultants ensure that clinical trial documentation is clear, concise, scientifically and medically accurate, and fully compliant with regulatory requirements.

Our medical writers, all with a degree in medicine, have extensive backgrounds in most therapeutic areas.

Services include:

  • Clinical development plans
  • Phase I-IV Protocols
  • Phase I-IV integrated clinical statistical report
  • Abstracts, manuscripts, and journal articles (peer reviewed journals)
  • Medical and scientific literature reviews
  • Investigator brochures
  • Informed consent form
  • Patient safety narrative


Our Phase I-IV integrated clinical statistical reports also include accurate appendices according to the ICH or client's guidelines. Clinical study reports can be consolidated into a single file and can be released electronically as Word or Acrobat PDF including hyperlinked table of contents or PDF bookmarks.

Site last updated: Tuesday 06 May 2014, 13:31
SPARC Consulting Srl - Via Archimede 94 - 20129 Milano
Tel. (+39) 02 43119667 - Fax (+39) 02 87071294 -
P.iva/C.F./Numero iscrizione Registro delle Imprese di Milano: 07616020967 - REA: MI-1971208 - Capitale sociale: 27.000 euro I.V.
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