Our regulatory and clinical medical writers are scientifically trained and apply the principles of clinical research in developing documents and submissions that effectively and clearly describe your research results, product use, and other medical information. They can develop and assist on any of the five modules of the Common Technical Document used for regulatory submission and communication. All of our regulatory and clinical medical writers are paired with a scientist or physician to ensure thoroughness, accuracy and final quality of the various written materials. Typical writing efforts include:
|
|