Regulatory writing and QC auditing

Smartsource your clinical research documentation to our team of regulatory experts. Our regulatory writers have a thorough understanding of regulatory processes and guidelines. They will be able to work with your templates, style guides, document systems, and internal processes within your time schedules and budget. CACTUS clinical research documentation services include but are not limited to the following:

• Clinical study reports
• Summary and overview documents
• Investigator brochures
• Development safety update reports
• Patient narratives
• Protocols
• QC auditing