Medical Writing

The Frontage medical writing team includes experienced clinical scientists and medical writers who are skilled at data interpretation and the clear and effective communication of your scientific results. You benefit from writers who possess extensive knowledge of the pathophysiology and treatment of diseases, as well as the ability to rapidly assimilate new scientific information for novel technologies.

 

For documents ranging from protocols to regulatory submissions, Frontage uses an integrated, multidisciplinary, project team approach, including key members from the sponsor and investigators or outside experts where applicable. This team meets on a frequent basis from project initiation to completion. 

 

Frontage Medical Writing services include:

 

  • Phase I-IV protocols
  • Phase I-IV case report forms (CRFs)
  • Global clinical trial applications
  • Drug, device and biologic marketing applications
  • Preclinical and scientific reports
  • Investigator brochures
  • Premarketing and post-approval annual reports
  • Patient safety narratives
  • FDA briefing documents