The three main stakeholders in our medical writing department are medical writers, regulatory experts and scientific affairs. Our team has expertise is various writing styles and formats always ensuring compliance with ICH-GCP with both client templates and/or our templates We provide individual project writing as well as full writing service.



We concentrate of the following aspects of writing:

  • Clinical Protocols and SOPs
  • Clinical Study Reports
  • SOPs
  • Expert Reports/Clinical Overviews
  • Informed Consent Documents
  • Investigator Brochures
  • Ethics communications
  • Summaries of literature
  • Patient Information Sheets
  • Regulatory and Ethics reporting
  • Drug Safety Reports