Medical Writing

C3 Research has outstanding resources to provide medical, regulatory, scientific and technical writing support to create clear and effective documents for any stage of development. Whether it is creating a new document from our library of resources or finalizing a document to comply with current industry standards, our team brings the technical experience needed to draft the research documents at the highest levels of quality, including:

  • Regulatory filing documents, including INDs
  • Investigator Brochures (IB)
  • Clinical protocol development
  • Clinical protocol amendments
  • Informed consent forms
  • Annual safety reports
  • Instructions for use (IFU)
  • Clinical study reports (CSR)
  • Scientific manuscripts, posters and publications