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