Medical Writing

Clinilabs employs a number of veteran medical writers with advanced degrees and diverse therapeutic area experience. Writing assignments are given to writers who are subject matter experts; writers who work closely with clients to ensure that documents meet expectations. From project inception to the delivery of the final clinical study report, our team is available to provide exceptional medical, technical, and regulatory writing services. Writers work with our own templates or yours to create the documents needed for any Phase I or Phase II clinical trial. We have experience in the production of the following documents:

  • Clinical study synopses
  • Clinical study protocols
  • Protocol amendments
  • Investigator brochures
  • Clinical study reports
  • Informed consent forms
  • Clinical study report verification
  • Case report forms
  • Patient information sheets



Click HERE to download our Multicenter, Full Service CRO Case Study.