Medical Writing

Our team comprises of tenured clinical research professionals and communications specialists who are GCP trained. We provide expertise across a wide range of therapeutic areas and incorporate our collective international know-how to facilitate ready acceptance of our documents by different regulatory authorities and independent ethics committees/boards.

When developing such documents we ensure painstakingly that the scientific integrity is articulated in clear fashion ensuring that the messaging resonates with the target reading audience and each document is QC’d before finalization.

Examples of the documents that we can develop are:

  • clinical trial protocols
  • investigator’s brochuresinformed consent form / informed assent form
  • clinical study reportsclinical summaries
  • patient compliance tools
  • patient information sheet

For further information contact us to see how our expertise can service you.