Medical Writing

Good science, written well

The end result of a clinical study, a written report, remains as a record and summary of the clinical investigation long after study teams, investigators and patients have moved on. Meticulous planning, starting with good science and appropriate research questions, and ethical production of all written study materials is fundamental to the quality of the final output of a project.

You can count on our experienced medical writers to cover all your documentation and reporting needs – from clinical trial protocols and amendments, development safety update reports and integrated clinical study reports. Thorough but fast, our expert writers deliver quality documentation to tight deadlines.

Simply contact us to discover just how our medical writers can support you.

The words you’re looking for – Our medical team combines qualified expertise and in-depth experience.

  • Clinical trial protocols and protocol amendments
  • Subject information and informed consent forms (ICFs)
  • Integrated clinical and statistical reports meeting global regulatory requirements
  • Observation plans and final reports for post-marketing studies
  • Development safety update reports (DSURs)
  • Paediatric investigation plans (PIPs)
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