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