Specialist services in medical writing to support your clinical trial

Medical and regulatory documentation developed by experienced medical writing teams plays a pivotal role in the success of a clinical research project. Our professional service encompassing all regulatory requirements will be tailored to your needs.

Our medical writing team works closely with key operational departments including BiostatisticsMedical Affairs, Quality Assurance, Regulatory and Clinical Operations to access a fully integrated network of information.

Single point of contact

Each project is assigned a medical writer who is responsible for managing the writing process. A communication plan is drawn up to ensure you are aware of progress against timelines.

Our rigorous quality assurance process ensures all regulatory requirements are met and that you are provided with a professional, efficient service. We offer certified translations of all medical writing services for our projects globally.

Full range of services

We offer a complete writing service spanning from individual documents to extensive medical writing programs. Our medical writers have the therapeutic expertise and knowledge to deliver quality materials according to your specifications.

Regulatory publishing

  • Regulatory writing
  • Regulatory agency submissions

Clinical studies

  • Clinical study reports
  • Study protocols, amendments, and administrative changes


  • Publications, posters, and abstracts
  • Promotional and educational material

Other medical writing services

  • Investigator brochures
  • Patient narratives
  • Aggregate reports
  • Product labelling

ICON also provides a range of Medical Communications and Creative and Digital Services to support product brand success.