CROS NT provides medical writing services focused on converting the complexity of trial information into clear and understandable clinical study documentation for Phase I-IV clinical trials and medical device studies.

CROS NT Medical Writing Team
We have a global team of Medical Writers, all of which are native or fluent English speakers, and several have bilingual writing capabilities. These Medical Writers have produced technical and scientific documentation for all types of studies for both the EMA and FDA. Our team has experience in over 40 therapeutic areas and hundreds of indications.

We can write your:

  • Protocol
  • EMA and FDA Briefing Packages
  • Investigator Brochure
  • Clinical Study Reports (CSR)
  • Marketing Documentation
  • Posters and/or Abstracts
  • Customized reports based on client requests