Good science, written well



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

You can count on our experienced medical writers to cover all your documentation and reporting needs, including clinical trial protocols and amendments, development safety update reports and integrated clinical study reports. Fast yet thorough, our expert writers deliver quality documentation within tight deadlines.

To discover just how our medical writers can support you:


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  • Clinical trial protocols and protocol amendments

  • Subject information and informed consent forms (ICFs)

  • Integrated clinical trial report meeting global regulatory requirements

  • Observation plans and final reports for post-marketing studies

  • Development safety update reports (DSURs)

  • Paediatric investigation plans (PIPs)